Patterning and alteration of molecules

ABSTRACT

The present invention provides a series of methods, compositions, and articles for patterning a surface with multiple, aligned layers of molecules, by exposing the molecules to electromagnetic radiation. In certain embodiments, a single photomask acts as an area-selective filter for light at multiple wavelengths. A single set of exposures of multiple wavelengths through this photomask may make it possible to fabricate a pattern comprising discontinuous multiple regions, where the regions differ from each other in at least one chemical and/or physical property, without acts of alignment between the exposures. In certain embodiments, the surface includes molecules attached thereto that can be photocleaved upon exposure to a certain wavelength of radiation, thereby altering the chemical composition on at least a portion of the surface. In some embodiments, the molecules attached to the surface may include thiol moieties (e.g., as in alkanethiol), by which the molecule can become attached to the surface. In some embodiments, the molecules may be terminated at the unattached end with photocleavable groups. In other embodiments, a molecule that was photocleaved may be exposed to another molecule that binds to the photocleaved molecule. In certain cases, the molecules may be terminated at the unattached end with hydrophilic groups that may, for example, be resistant to the adsorption of proteins. In other cases, the molecules may be terminated at the unattached end with end groups that are not resistant to the adsorption of proteins. In certain embodiments, the techniques are used to pattern simultaneously two different regions that are resistant to the adsorption of proteins, and a third region that does not resist the adsorption of proteins.

RELATED APPLICATIONS

This application claims priority under 35 U.S.C. § 119(e) to U.S.Provisional Application Ser. No. 60/622,187, entitled “Patterning andAlternation of Molecules,” filed on Oct. 26, 2004.

FEDERALLY SPONSORED RESEARCH

Various aspects of the present invention were supported by a grant fromthe National Institutes of Health (No. GM065364). The Government mayhave certain rights in the invention.

FIELD OF THE INVENTION

This invention generally relates to the alteration of the molecules of asurface, and more specifically, to the alteration of the molecules of asurface by photocleavage of the molecules.

BACKGROUND

The ability to produce complex patterns of molecules on surfaces isimportant for understanding a number of different phenomena includingdewetting, adhesion, cell-surface interactions, and cell-cellinteractions; it is also significant for developing applications inbiology and biochemistry, such as assays, microarrays, and devices forhigh-throughput screening.

Several techniques allow the alignment of molecules, and in particular,the alignment of SAMs, on surfaces. Microcontact printing (μCP) ofalkanethiols on a gold or silver surface using a poly(dimethylsiloxane)(PDMS) stamp allows one type of alkanethiol SAM to be patterned in thebackground of a second type of alkanethiol. Multiple printing steps canproduce multiple patterns of molecules on a surface, but most patternsrequire the alignment of a stamp. Micromolding in capillaries (MIMIC) isa general method for depositing polymers, SAMs, and proteins incontinuous patterns on a substrate, but MIMIC is unable to alignmultiple, discontinuous patterns. Three-dimensional networks of channelsin PDMS can generate multiple, discontinuous patterns of proteins andcells, but the microfluidic networks require alignment in fabrication.Chen et al. have demonstrated an elegant technique using a multilevelPDMS stamp to print multiple, aligned regions of proteins. Thistechnique involves several complicated steps (in fabrication of thestamp, in inking, and in printing or patterning).

A number of procedures for multicolor patterning have usedphotolithography. In one report, different fluorescent dyes were coupledin solution to a surface coated with bovine serum albumin (BSA) usingirradiation with UV light through a photomask. Where light passedthrough the photomask, the fluorescent dye molecules were excited andproduced radicals; fluorescent dye radical molecules coupled to BSA inregions defined mostly by the pattern of illumination. Although thismethod permitted multiple molecules to be patterned by using differentwavelengths to excite different fluorescent dyes, alignment ofindividual patterns was not demonstrated, and the resolution of thefeatures was limited by the diffusion of the fluorescent dyes. Anotherreport described the use of diarylethene derivatives that undergophotoinduced structural rearrangements depending on the wavelength oflight used. Two diarylethene derivatives were cast as a film and exposedsequentially through individual masks to UV or visible light.

The examples above show that many existing techniques require alignmentof two (or more) features when fabricating either a photomask or amicrofluidic device (e.g., photolithography, MIMIC) or alignment of astamp when printing patterns of molecules (e.g., CP, microcontactprinting), in order to fabricate multiple patterns of molecules on asurface. There remains a general need in the art for improved methods offabricating multiple patterns on a surface, without multiple steps ofalignment.

SUMMARY OF THE INVENTION

This invention relates to the alteration of the molecules of a surfaceby photocleavage of the molecules. The subject matter of the presentinvention involves, in some cases, interrelated products, alternativesolutions to a particular problem, and/or a plurality of different usesof one or more systems and/or articles.

One aspect of the invention provides a method. In one set ofembodiments, the method includes acts of providing a surface, at least aportion of which comprises molecules attached thereon, exposing thesurface to electromagnetic radiation, and altering the layer ofmolecules with the electromagnetic radiation to form a patterncomprising at least a first, second, and third region, where the first,second, and third regions differ from each other in at least onechemical and/or physical characteristic. In another set of embodiments,the method includes an act of reacting a photocleavable moiety toproduce a SAM-forming species comprising the photocleavable moiety.

Another aspect of the invention provides a composition. The composition,according to one set of embodiments, includes a compound having astructure:X—R-Q,where X is an attachment moiety able to chemically bind a surface, Qcomprises a photocleavable moiety, and R is a moiety connecting X and Q.

In another set of embodiments, the composition comprises a SAM-formingspecies comprising a photocleavable moiety, where the SAM-formingspecies is free from attachment to a surface.

Yet another aspect of the invention provides an article. According toone set of embodiments, the article comprises

where | comprises a surface, X is an attachment moiety able tochemically bind a surface, Q comprises a photocleavable moiety, and R isa moiety connecting X and Q. In some cases,

is not:

In another embodiment, the present invention is directed to a photomaskcomprising a first region that is transparent to light at a firstwavelength within a first range, and opaque to other wavelengths oflight not within this range; a second region that is transparent tolight at a second wavelength within a second range, and opaque to otherwavelengths of light not within this range, wherein the first and secondwavelengths differ, and a third region that is opaque to wavelengths oflight in at least the first and second ranges.

In another aspect, the present invention is directed to a method ofmaking one or more of the embodiments described herein. In yet anotheraspect, the present invention is directed to a method of using one ormore of the embodiments described herein. In still another aspect, thepresent invention is directed to a method of promoting one or more ofthe embodiments described herein.

Other advantages and novel features of the present invention will becomeapparent from the following detailed description of various non-limitingembodiments of the invention when considered in conjunction with theaccompanying figures. In cases where the present specification and adocument incorporated by reference include conflicting and/orinconsistent disclosure, the present specification shall control. If twoor more documents incorporated by reference include conflicting and/orinconsistent disclosure with respect to each other, then the documenthaving the later effective date shall control.

BRIEF DESCRIPTION OF THE DRAWINGS

Non-limiting embodiments of the present invention will be described byway of example with reference to the accompanying figures, which areschematic and are not intended to be drawn to scale. In the figures,each identical or nearly identical component illustrated is typicallyrepresented by a single numeral. For purposes of clarity, not everycomponent is labeled in every figure, nor is every component of eachembodiment of the invention shown where illustration is not necessary toallow those of ordinary skill in the art to understand the invention. Inthe figures:

FIG. 1 is a schematic illustration showing patterning of a goldsubstrate with multiple, aligned SAMs using a photomask. Two methods aredescribed: the photopatterning method described by process A (FIG. 1A)produces a SAM that terminates in amines after exposure to light at 365nm, while the method described by process B (FIG. 1B) produces a SAMthat terminates in primary amides after exposure to light at 365 nm. Themethod described by process B also permits the original SAM to presentarbitrary functionality beyond the photocleavable linker. A new SAM canbe formed in regions that are exposed to light at 220 nm in bothapproaches. R represents any group that can be coupled to a carboxylicacid, e.g., amine, alcohol, etc.; R′ represents any group that containsa carboxylic acid, aldehyde, etc. that can be coupled to an amine; R″represents an arbitrary functionality that terminates with a thiolgroup. (Note: alkanethiol SAMs on gold substrates are tilted 30° to thenormal and are shown here schematically without any tilt.)

FIG. 2 is a schematic illustration showing synthetic strategies for (A)HS(CH₂)₁₁(EG₂)NPOC and HS(CH₂)₁₁(EG₂)DNP and for (B)HS(CH₂)₁₁EG₆NPOP(GRGD) (on a solid-phase support).

FIG. 3 illustrates fabrication and characterization of a photomask. FIG.3A shows the transmission spectra of each component used in the mask.Chromium is sufficiently opaque to prevent significant transmission oflight at 220 or 365 nm. Indium tin oxide is sufficiently transparent tolight at 365 nm and opaque to light at 220 nm to filter deep UVwavelengths during exposure. Quartz is transparent to light at allwavelengths used in this study. FIG. 3B is a schematic illustrationshowing the procedure used for fabricating a photomask that allowsarea-selective transmission of 220 nm light, 365 nm light, and neitherof these wavelengths.

FIG. 4 illustrates the preparation and immunolabeling of multiple,aligned SAMs. FIG. 4A is a schematic illustration of patterningmultiple, aligned SAMs using a photomask. Using the strategy outlined inFIG. 1A, a mixed SAM containing HS(CH₂)₁₁EG₂NPOC and HS(CH₂)₁₁EG₆OH wasilluminated through an area-selective mask that transmitted light eitherat 220 or 365 nm only or that blocked light at all wavelengths, toproduce a region containing the original SAM, a SAM that terminated inprimary amines, and a region of bare gold (or oxidized gold). (+)-biotinN-hydroxysuccinimide ester was allowed to react with the primary aminesand also formed a new SAM composed of HS(CH₂)₁₁EG₂DNP and HS(CH₂)₁₁EG₆OHon the exposed gold. SAMs were labeled using anti-biotin mouse IgG(followed by fluorescently labeled anti-mouse IgG) and anti-DNP rabbitIgG (followed by fluorescently labeled anti-rabbit IgG). FIG. 4B arefluorescence images of patterns of multiple, aligned SAMs.

FIG. 5 shows the fabrication and characterization of surfaces containingtwo SAMs that resist the adsorption of proteins and a surface that doesnot resist the adsorption of proteins. FIG. 5A is a schematicillustration of the approach used to pattern multiple, aligned SAMs thatresist the adsorption of proteins. Using the strategy outlined in FIG.1B, a mixed SAM containing HS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH wasilluminate through an area-selective mask that transmits selectivelylight at 220 or 365 nm or blocks light at these wavelengths, to producea bare gold (or oxidized gold) region, a SAM that terminates in primaryamides, and a region containing the original SAM. FIG. 5B is an SPRsensorgram of the mixed SAMs for substrates that have not been exposedto light, that have been exposed to light at 365 nm, and that have beenexposed to light at 220 nm. The original SAM, protected from exposure tolight by the opaque, chromium area of the mask, remains resistant to theadsorption of fibrinogen (1 mg/mL, PBS buffer). After exposure to lightat 365 nm, the SAM region that terminates in primary amides resists theadsorption of proteins, and after exposure to light at 220 nm, the gold(or oxidized gold) surface (the monolayer is cleaved entirely) is unableto resist the adsorption of proteins.

FIG. 6 shows MALDI-TOF mass spectra of samples containing mixed SAMsthat have not been exposed to light, that have been exposed to light at365 nm, and that have been exposed to light at 220 nm. The peak at m/z958 (I) corresponded to the symmetric disulfideHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆OH that is expected to be abundant in thespectra of the mixed SAMs. The initial monolayer displayed a peak at m/z1659 (II) corresponding to the asymmetric disulfideHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD) (expected m/z is 1659). Afterexposure to light at 365 nm, a peak at m/z 1015 (III) corresponding tothe asymmetric disulfide HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂ (expected m/z is992 plus Na⁺, m/z 23, gives m/z 1015) was observed. After exposure tolight at 220 nm, no peaks were observed, indicating photocleavage of themixed SAM. No other molecular fragments are expected to be insignificant abundance in this region (800<m/z<2000) for all threespectra, in agreement with the observed data. The symmetric disulfides(GRGD)NPOPEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD) andH₂NOCEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂ are unlikely to appear in the massspectra because of the dilute concentration of the alkanethiolHS(CH₂)₁₁EG₆NPOP(GRGD) present in the original mixed SAM. Althoughindividual alkanethiols corresponding to HS(CH₂)₁₁EG₆NPOP(GRGD) andHS(CH₂)₁₁EG₆CONH₂ were observed occasionally, most molecular fragmentsappeared as disulfides.

FIG. 7 shows the patterning two aligned SAMs that resist the adsorptionof proteins and a third region that does not resist the adsorption ofproteins. FIG. 7A is a representation of the expected pattern ofmultiple, aligned SAMs generated from a mixed SAM containingHS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH. FIG. 7B is a spatiallyresolved image of multiple, aligned SAMs constructed from the locationof m/z peaks obtained using MALDI-TOF and corresponding toHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD) (white),HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂ (gray), or no alkanethiol (black). Thespatial resolution of our detector is limited to 100 μm.

FIG. 8 is a photograph of a surface comprising alkanethiols that wasused as an etch resist. The continuous gold film represents a regionprotected from light at 220 nm and 365 nm. The partial gold filmrepresents a region protected only from 220 nm light, and shows somedegree of etching. The chrome/silicon region represents a region exposedto light at 220 nm and 365 nm. Exposure times are as for the publishedarticle. Scale bar is 100 microns.

DETAILED DESCRIPTION

The present invention provides a series of methods, compositions, andarticles for patterning a surface with multiple patterned regions thatmay differ from each other in at least one chemical and/or physicalcharacteristic. Certain embodiments, as described in more detail below,and methods described herein can be utilized to fabricate surfaceshaving discreet, non-continuous patterns thereon that differ from eachother with regard to their ability to interact with other substances andmaterials to which they are exposed. For instance, in certainembodiments, an article derived from practicing a method as describedherein can result in a patterned surface characterized by at leastfirst, second, and third regions that differ from each other in, forexample, their hydrophobicity, ability to resist or promote binding ofproteins, cytophilicity (i.e. ability to bind or resist binding ofcells), and/or their ability to be etched or otherwise reacted byexposure to the solution containing a reactant, for example, an etchingsolution.

Various aspects of the invention provide methods, compositions, andarticles for patterning a surface with molecules, for example multiple,aligned layers of molecules, by exposing the molecules toelectromagnetic radiation. In certain embodiments, a single photomaskacts as an area-selective filter for light at multiple wavelengths. Asingle set of exposures of multiple wavelengths through this photomaskmay make it possible to fabricate a pattern comprising discontinuousmultiple regions, where the regions differ from each other in at leastone chemical and/or physical property, without acts of alignment betweenthe exposures. In certain embodiments, the surface includes moleculesattached thereto that can be photocleaved upon exposure to a certainwavelength of radiation, thereby altering the chemical composition on atleast a portion of the surface. In some embodiments, the moleculesattached to the surface may include thiol moieties (e.g., as inalkanethiol), by which the molecule can become attached to the surface.In some embodiments, the molecules may be terminated at the unattachedend with photocleavable groups. In other embodiments, a molecule thatwas photocleaved may be exposed to another molecule that binds to thephotocleaved molecule. In certain cases, the molecules may be terminatedat the unattached end with hydrophilic groups that may, for example, beresistant to the adsorption of proteins. In other cases, the moleculesmay be terminated at the unattached end with end groups that are notresistant to the adsorption of proteins. In certain embodiments, thetechniques are used to pattern simultaneously two different regions thatare resistant to the adsorption of proteins, and a third region thatdoes not resist the adsorption of proteins.

As described in more detail below, articles comprising patternedsurfaces as produced according to certain embodiments of the inventioncan be utilized in a very wide variety of applications requiring orbenefiting from patterned surfaces including multiple regionscomprising, in certain instances, non-continuous patterns havingsmallest feature sizes on the order of less than 1 millimeter, certainembodiments less than 100 microns, in other embodiments less than 10microns, in yet other embodiments less than 1 micron, and in otherembodiments on the scale of tens or hundreds of nanometers. The methodsdisclosed in more detail below can be utilized to form patterns onmaterial surfaces comprised of an extremely wide variety of materials,as will become apparent to those of ordinary skill in the art. Alsodisclosed and provided herein are inventive photomask articles that canbe, as described further below, utilized to form patterned layers ormonolayers or self-assembled monolayers (SAMs) on material surfaces; toform patterns of inorganic materials on surfaces; to form patterns oforganic and/or biological materials on surfaces; to form patterns onsurfaces via contacting the surfaces with the material that chemicallyreacts with and/or creates/etches the material surface; etc. The abilityof the present invention to, in certain embodiments, form patternedsurfaces is, in certain respects, somewhat similar to known techniquesof patterning surfaces via microstamping and soft lithography (see,e.g., International Patent Application No. PCT/US01/17246, filed May 25,2001, entitled “Patterning of Surfaces Utilizing Microfluidic StampsIncluding Three-Dimensionally Arrayed Channel Networks,” by Anderson, etal., published as WO 01/89788 International Patent Application No.PCT/US2004/002498, filed Jan. 29, 2004, entitled “Alteration of SurfaceAffinities,” by Jiang, et al., each incorporated herein by reference. Avariety of such materials and applications is described in detail inU.S. Pat. Nos. 5,512,131; 5,620,850; 5,776,748; 5,900,160; 5,951,881;and 5,976,826, each of which is incorporated herein by reference).

In certain embodiments of the invention, a surface comprising aplurality of chemical chains including two or more differentcompositions can be formed. E.g., in the case of SAMs, a monolayer maycomprise a first chemical chain and a second chemical chain having adifferent composition from the first chemical chain. This mixture ofdifferent compositions is referred to as a “mixed SAM”. Mixed SAMs allowa surface to be tailored for a particular application. For example, somemixed SAMs show resistance to protein adsorption when present in anamount as low as 25% of the total of chemical chains. Of course, threeor more different SAM types can be readily contemplated.

As will become more apparent in the discussion below, certainembodiments of the inventive methods and articles provided according tothe present invention can provide several advantages over traditionalmicrostamping and other soft lithography techniques. For example,certain methods disclosed herein have the ability to form patternscomprising at least three distinct regions, each of which ischaracterized by a different set of chemical and/or physical properties,for example, in certain embodiments, by the presence on a surface ofdifferent molecular species. Typical soft lithography techniques arecapable of patterning only two types of molecules on the surface,especially for applications wherein the patterned molecules comprisealigned molecules, such as SAMs. In certain embodiments, wherein patternformation is effected via exposing a surface of an article toelectromagnetic radiation, such as light, through a wavelength-selective patterned photomask, the inventive methods can providefor the formation of patterns comprising multiple discreet regionswithout the need for realignment of a photomask between exposures of thesurface to the electromagnetic radiation, and, in certain instances, canprovide for the formation of each of the discreet regions of the patternsimultaneously with a single exposure to the electromagnetic radiation.As previously eluded to above, articles comprising patterned surfacessuch as can be fabricated according to certain embodiments of thepresent invention may be utilized in a wide variety of applications, forexample, for use in biochemical assays, as microarrays (e.g. forproteomics and/or geonomics); as gene-chips; as MEMS devices; or assubstrates for use in applications involving differential etchingchemistry.

In one particular set of embodiments, the inventive articles providedaccording to certain embodiments of the inventions, because it ispossible to create arbitrarily complex patterns comprising a largenumber of patterned regions containing different patterned molecularspecies, articles divided according to certain of the inventive methodspotentially having extremely wide range of use for cellularmanipulation, drug screening (e.g. utilizing cell-based drug screeningassays); studies of cell-signaling; studies of cell morphology andarchitecture as it relates to function; etc. For example, in oneexemplary application, the inventive articles can provide a patternedsurface having the ability to bind to cells and/or proteins to differentdegrees for different regions. In such an example, proteins, forexample, can be selectively patterned onto a surface which are adhesiveto cells, non-adhesive to cells, or selectively adhesive to certaincells while non-adhesive to other cells. By forming patterns with suchproteins, or other cell-binding molecules, complex patterns of one celltype or a variety of cell types can be selectively patterned ontosurfaces for various applications, for example, for forming biosensorsor performing drug screening tests. Using the methods disclosed below,it is possible to pattern a large number of different cell types, eachseparated from each other and arranged in a patterned array format. Suchpatterning can be accomplished, according to certain embodiments of theinvention, by, for example, coating a surface with a surface coating,for example, a SAM, in certain embodiments comprising a SAM-formingmolecule that is bound to the surface that includes as part of itsstructure a photocleavable moiety, exposing the surface, for example,through a photomask, to electromagnetic radiation, and altering thelayer of molecules on the surface with the electromagnetic radiation toform a pattern comprising multiple regions, in certain embodiments atleast first, second, and: third regions, that differ from each other intheir ability to adhere proteins and/or cells. Such ability to formpatterns comprising arrays of regions, with each region including aparticular cell, protein, molecular species type or mixture of cell,protein, molecular species types, can enable the creation of materialsurfaces for use of biosensors or drug screening devices having cells orother materials patterned thereon that can be easily and readilyidentified by their spatial locations on the surface.

As mentioned above and as described in much more detail below, certainembodiments of the inventive methods can form an article having apatterned surface by exposing a surface which comprises a layer ofmolecules attached thereon to electromagnetic radiation, for examplethrough a wavelength and area selective photomask, such that the layerof molecules in different regions are differentially altered by theelectromagnetic radiation to form a pattern comprising discreet regionseach having a different chemical property, for example characterized bya different molecular species attached to the surface in such region. Incertain such embodiments, the layer of molecules attached to the surfacethat are modified via exposure to the electromagnetic radiation areformed via attachment to the surface of molecular species, such asSAM-forming species, which have a structure comprising a moiety able toattach to a particular surface or substrate (e.g. a thiol moiety formetallic surfaces such as gold, silver, copper, or other noble metals, asaline moiety for attachment to silicon atom-containing surfaces such asglass, or a wide variety of other attachment moieties as mentionedbelow), connected, for example via a linker such as an alkyl moiety, toa photocleavable moiety, which is able to be cleaved by exposure toelectromagnetic radiation, such as light, at a wavelength and/orintensity that is not able to cleave other bonds within the moleculeattached to the surface. A wide variety of such molecular speciesincluding photocleavable moieties, for example SAM-forming species aredescribed in much more detail below.

In one aspect of the present invention, inventive SAM-forming speciesare provided, as described in much more detail below, which comprise aphotocleavable moiety. Advantageously, and according to certainembodiments of the invention, such SAM-forming species are synthesizedin solution and free from attachment to a surface. Such SAM-formingspecies may then be deposited onto surfaces of articles and attachedthereto via appropriate selection of an attachment moiety of theSAM-forming species. In certain embodiments, the inventive SAM-formingspecies comprise alkanethiols comprising one or more photocleavablemoieties (see FIGS. 1, 4, 5 and associated discussion below), which arewell suited for attachment to gold-containing surfaces. It is known thatthat thiol-gold bond connecting alkanethiols to the gold-containingsurface can be ruptured, freeing the alkanethiol from the surface, viaexposure to light at about 220 nm. Certain aspects of the presentinvention provide the provision of alkanethiol species attached to agold surface that include a photocleavable moiety, for example, any oneof a variety of photocleavable amine-protecting groups or photocleavablelinkers known to those of skill in the art and described in greaterdetail below, which have the ability to be cleaved at wavelengths thatare greater than the 220 nm able to cleave the gold thiol bond and atwavelengths that are unable to cause cleavage of other bonds within themolecule. Accordingly, in such embodiments, by exposing a surface coatedwith the SAM comprising such photocleavable alkanethiols, differentiallypattern regions can be formed by exposing such surface to light througha photomask (see, for example, FIG. 1A and 1B) having first regions(left most regions in the Figures) that are essentially opaque to lightat all relevant wavelengths from a source of light, second patternregions (gray central regions in the Figures) that are configured totransmit light at a wavelength able to cleave the photocleavable moiety(e.g. 365 nm for the photocleavable moieties illustrated in FIG. 1) butnot cleave the sulfur gold surface bond and release the entirealkanethiol from the surface, and third regions (white regions in theFigures) that are configured to transmit light at a wavelength that isable to cleave the entire alkanethiol from the surface. Althoughphotocleavable groups having sensitivity to light at 365 nm areexemplified in FIG. 1 and alkanethiols have been used in conjunctionwith gold surfaces wherein association of the alkanethiols from thesurface can be effected by exposure to light at 220 nm., it should beunderstood that in other embodiments, photocleavable moieties and/orsurface-attachment moiety combinations can be chosen such that they aresensitive to cleavage at other wavelengths of light, and/or other types,wavelengths, intensities, etc. of electromagnetic radiation. A varietyof such alternative materials could be envisioned by those of ordinaryskill in the art in view of the present teachings and applied using nomore than routine testing and experimentation.

As illustrated in FIG. 1, exposure of a surface coated withphotocleavable alkanethiols, such as those discussed above, uponexposure to light at the first and second wavelengths through thephotomask is characterized by a pattern comprising three discreetregions having a surface which, attached thereto are different molecularspecies, or no molecular species. In the embodiment illustrated in FIG.1A, for example, exposure to light at 365 nm and 220 nm through thephotomask results in a first region (left), which has not exposed tolight at either 365 or 220 nm and which comprises attached thereto thecomplete alkanethiol originally present on the surface; second regions(center) exposed to light at 365 nm, but not 220 nm, which compriseattached thereto a cleavage product of the originally presentphotocleavable SAM-forming species which, in the illustrated embodiment,provides a terminal group comprising a reactive functionality (a aminegroup is illustrated) and is terminus. Of course, in other embodiments,determines of the cleaved molecular species could comprise any of a widevariety of other functionalities including, but not limited, carboxylicacids, alcohols, aldehydes, amides (e.g. see FIG. 5); and a third region(right) exposed to light at 220 nm from which the entire alkanethiolmoiety has been cleaved exposing the underlying surface of thesubstrate. If desired, in certain embodiments as illustrated in FIG. 1,after exposure to electromagnetic radiation resulting in thedifferential pattern formation, the surface of the article may beexposed to and reacted with other species that are able to bind to oneor more of the patterned regions (e.g., are able to react with theterminal functionality of the cleaved photocleavable alkanethiol or areable to react with the exposed substrate surface). In other embodiments,more complex patterns could be created utilizing additional regions ofattachment of molecular species having differing photocleavable moietiesand/or attachment moieties sensitive to wavelengths and/or intensitiesof electromagnetic radiation of differing values. In yet otherembodiments, additional pattern formation flexibility could be achievedby providing coatings, for example, SAMs comprising photocleavablemolecular species having more than one photocleavable moiety presentwithin the structure, which are each able to be cleaved at differentwavelengths, intensities, etc. In certain embodiments of the inventivemethods involving patterning surfaces having attached thereto via aphotosensitive attachment moiety molecular species comprising aphotocleaveable group, such as, for example, a photocleavable SAM suchas a photocleavable alkanethiol, it can be advantageous to utilizephotocleaveable molecular species including a photocleavable moiety thatis able to be cleaved with light of a wavelength exceeding thewavelength required to cleave the bond directly attaching the molecularspecies to the substrate surface. For example, in the case ofalkanethiols in which the sulfur-surface bond is typically able to becleaved utilizing light at a wavelength of about 220 nm, it ispreferable to include a photocleavable moiety in such a molecularspecies that is able to be cleaved with light having a first wavelengthgreater than this, for example at least about 250 nm. In addition,because at wavelengths below about 200 nm carbon-carbon and otherintermolecular bonds are often able to be cleaved more or less atrandom, it can be advantageous to utilize an attachment moiety in amolecular species to be coded onto a surface that is able to be cleavedat a wavelength less than the wavelength able to cleave thephotocleavable moiety but greater than the wavelength able toindiscriminately rupture molecular bonds. Such election can increase theselectivity of bond rupture and result in more predictable and “clean”cleavage of molecular species from a surface. For example, in certainembodiments, it can be advantageous to utilize a molecular species, suchas SAM-forming species, that becomes bound to a surface via a bond thatis able to be cleaved with light having a wavelength of at least about200 nm, but less than the wavelength of any other photocleavable moietypresent within the molecular species. In certain embodiments, it can beadvantageous to utilize SAM-forming species for attachment to surfacesto be patterned that do not require presence of scavenger moleculesduring photocleavage. A variety of such species and photocleavablemoieties are known in the art and are described in more detail below inthe context of the appended examples. In general, described in muchgreater detail below, are a wide variety of useful or potentially usefulmolecular species, such as SAM-forming molecular species, such asalkanethiols, that are useful for practicing the above-describedembodiments of the invention.

As discussed above, certain embodiments of the present invention providepatterning methods and patterned articles that can have certainadvantages over those produced by conventional patterning techniques,such as soft lithography. For example, in certain embodiments of theinventive methods for forming pattern surfaces via exposure of a surfaceto electromagnetic radiations through a photomask, it is not necessaryto directly contact the surface with the photomask. By contrast,micro-stamping and other micro-contact soft lithography techniquesgenerally require contact of the stamping surface with a surface to bepatterned. Avoiding such contact, as can be accomplished via practicingcertain aspects of the present invention may be able to produce patternregions having greater uniformity, improved surface coverage, lack ofcontamination caused by exposure to the stamp material, etc. Inaddition, because, in certain embodiment, the invention provides forformation of patterns via exposure to electromagnetic radiation via arigid photomask, it may be possible to provide more consistent shapesand/or dimensions for pattern features and/or to achieve greaterresolution and small feature size. For example, certain embodiments, atleast one region of a pattern formed according to a method of thepresent invention via exposure of a surface to electromagnetic radiationresulting in modification of the surface to produce a pattern, a regionof the pattern being characterized by having a smaller cross-sectionaldimension not exceeding about 100 microns, and other embodiments notexceeding about 90 microns, 80 microns, 70 microns, 60 microns, 50microns, 40 microns, 30 microns, 20 microns, 10 microns, 5 microns, 1micron, 500 nm, 400 nm, or less. One aspect of the invention alsoprovides the novel photomask article figure to be utilized in thecontext of certain embodiments of the inventive methods. The inventivephotomask comprises a new type of photo lithography mask that isconfigured to provide different regions having the ability to transmitor block selective wavelength(s) of light within the ultravioletspectrum, which typically includes those wavelengths of light able tocleave chemical bonds, such as those present in photocleavable moietiesand/or attachment moieties connected to a surface according to certainembodiments of the invention. Fabrication methods and furthercharacteristics of the inventive photomask according to certainembodiments of the invention are discussed in more detail below andpresented in Example 2.

As described herein, in some aspects of the invention, the applicationof light (photons) to at least a portion of a substrate according tocertain embodiments of the invention can cause at least a portion of amolecule attached to at least a portion of the substrate to be cleavedfrom the molecule (“photocleaved”). A portion of the molecule thatreacts with light to cause cleavage of the molecule is a “photocleavablemoiety.” In some cases, the light has a wavelength selected to cleave aportion of the photocleavable moiety (e.g., a covalent bond) butinsufficient to cleave other covalent bonds in the molecule. Forexample, the light may have a wavelength of about 365 nm or about 220nm. In one aspect of the invention, the molecule attached to thesubstrate forms part of a self-assembled monolayer.

For example, in certain embodiments, the substrate may be exposed tolight selected to cause cleavage of a portion of a photocleavablemolecule. The substrate may be exposed to such light for at least about5 seconds, at least about 10 seconds, at least about 15 seconds, atleast about 30 seconds, or at least about 1 minute or more in somecases. In certain embodiments, the substrate may be exposed to suchlight for less than about 10 minutes, in some cases in less than about 5minutes, and in other cases in less than about 2 minutes. In some cases,the substrate may be exposed to such light for between about 5 secondsand about 3 minutes, in other cases between about 10 seconds and about 2minutes, in other cases between about 30 seconds and about 1 minute, andin still other cases between about 10 seconds and about 1 minute.

An “attached” molecule, as used herein, refers to one that issufficiently immobilized with respect to a surface or other entity suchthat it will not detach under typical conditions of use (i.e., by fluidmovement or thermal energy), without exposure to light selected to causedetachment of the molecule or a portion thereof.

The molecules attached to the substrate may be hydrophilic orhydrophobic in some cases, or the molecules may have an affinity toanother entity, as described above. In some cases, the substrate mayinclude more than one type of molecule thereon that can be photocleaved.For example, the substrate may include a first type of molecule that isphotocleaved the substrate is exposed to light having a first frequency,and a second type of molecule that does not detach when the substrate isexposed to the light having a first frequency, but is able to bephotocleaved when the substrate is exposed to a second frequency.

The present invention describes, in another set of embodiments, a methodfor patterning a surface comprising at least a first, second, and thirdregion of attached molecules, which differ in either chemical and/orphysical property, using one photomask and one set of exposures to lightat different wavelengths, but without alignment of photomasks (FIG. 1).In some embodiments, the regions of the first, second, and thirdregions, or any combination thereof, may be discontinuous. In somecases, the molecules attached to the substrate may be photocleaved uponexposure to a certain wavelength of radiation, thereby leaving at leasta portion of a molecular species on the surface. In other cases, themolecules attached to the substrate may be photocleaved entirely suchthat the bare surface is exposed.

In some cases, bonds can be photocleaved selectively in differentregions of a SAM using one or more masks, which may be able to transmitlight at some wavelengths and/or regions, and at least partially inhibitthe transmission of light at other wavelengths and/or regions. Forexample, in some cases, the mask may include holes, and/or the mask mayinclude regions which selectively allow the transmission of light havingcertain frequencies. A specific, non-limiting example, is an area andwavelength-selective mask (i.e., a photomask that transmits differentwavelengths in different areas). In some embodiments, the photomask isselective for transmitting light of about 365 nm through the mask, andgenerally opaque to light of other wavelengths. In another embodiment,the photomask is selective for transmitting light of about 220 nmthrough the mask, and generally opaque to light of other wavelengths. Inyet another embodiment, the photomask is selective for transmittinglight of about 365 nm and about 220 nm through the mask, and generallyopaque to light of other wavelengths. In still other embodiments, thetransmission of light through the photomask is not limited to thesewavelengths, but can include any number and combination of patterns andwavelength-selective regions, as is described herein.

Different wavelengths of light that pass through the photomask allowdifferent points of cleavage of a molecule species. In certainembodiments, a pattern may be formed via cleavage of at least a portionof a molecule species attached on the surface within a first region. Inanother embodiment, the point of cleavage of a molecular speciesattached on a surface may be different from a point of cleavage of themolecular species attached on the surface within the second region. Forexample, in one embodiment, light of 365 nm cleaves an amine-protectinggroup; in another embodiment, light at 220 nm removes the entire SAM(regardless of functionality) from the surface and produces a region ofunprotected gold. In some cases, a different SAM can be formed inregions that were exposed to light at 220 nm upon incubation with adifferent alkanethiol. In some cases, other entities such as molecules,proteins, or particles (such as nanoparticles) can react or bind to thesurface by exposing the molecule to particular regions of the surface.These entities may be presented to surface in any suitable form, such asin a solution, gas, or solid. SAMs in regions that are protected fromexposure to light at 220 and 365 nm remains intact, but may also undergoreaction or binding to the suitable entities described herein.

As a non-limiting example, a microfabricated mask can be used as anarea- and wavelength-selective filter in the patterning multiple,aligned SAMs. The fabrication of the photomask described herein may bemade using any methods or techniques, or any materials, that areavailable to those skilled in the art. For example, a mask can befabricated by using a commercially available quartz substrate coatedwith indium tin oxide (ITO) as the initial substrate. ITO blocks lightat 220 nm; quartz transmits light at 220 nm (FIG. 3A). Usingelectron-beam metal evaporation, films of either chromium or gold can bedeposited on the ITO to block light at 365 nm, in addition to light at220 nm. It should be understood that other substrates can be used, andother techniques to deposit metals or other materials on the substratemay be used to achieve the same or similar results. In addition, othermetals or materials may be deposited on the substrate to block ortransmit light at other wavelengths, and can be used for achieving thesame or similar purposes and/or results.

The feature size wherein at least one region of the pattern wascharacterized by a smallest cross-sectional dimension, produced by themethods herein, may be on the order of less than about 100 microns, lessthan about 10 microns, or less than about 1 micron (e.g., FIG. 4B). Theresolution of the features typically reflects the method used tofabricate the regions of the mask that transmitted light. In someembodiments, these regions can be fabricated by wet-etching ITO toexpose quartz. In other embodiments, alternative fabrication processesmay include dry-etching (e.g., deep reactive ion etching) or othermethods of producing a mask having similar results.

In some embodiments, a photocleavable linker was used to pattern twoaligned SAMs that are resistant to the adsorption of proteins and athird region that does not resist the adsorption of proteins.

Certain embodiments of the invention involve surfaces with SAMs attachedthereon. As used herein, the term “self-assembled monolayer” (SAM)refers to a relatively ordered assembly of molecules attached on asurface, in which the molecules are oriented approximately parallel toeach other and roughly perpendicular to the surface. The molecules maybe attached to the surface through a bond, for example, a metal-sulfurbond.

A SAM-forming molecule may be attached to the substrate by any of a widevariety of suitable mechanisms known in the art that result in stableSAM formation on the substrate. For example, in one series ofembodiments, the substrate and SAM-forming compound are selected suchthat the SAM-forming compound terminates at a first end in a functionalgroup that attaches to, and typically binds to, a surface of thesubstrate. As used herein, the terminology “end” of a compound includesboth the physical terminus of a molecule as well as any portion of amolecule available for forming a bond or other attachment with thesubstrate in a way that the compound can form a SAM on the substrate. A“bond,” as used herein in this context, broadly refers to any physicaland/or chemical attractive interaction between a first entity, such as amolecule, and another entity, such as the surface of the substrate,where the force of the attractive interaction is of the magnitude ofchemical bond forces and is generally sufficient to allow the firstentity to become immobilized with respect to the other entity. Someexamples of such “bonds” include, without limitation, a covalent bond, acoordinated bond, chemisorption (e.g., a metal-sulfur bond), hydrogenbonding, and the like. The affinity may also be characterized ascytophilic and/or cytophobic in nature, as further described below.

The compound may comprise, for example, a molecule having first andsecond terminal ends, separated by a spacer portion, the first terminalend comprising a first functional group selected to bond to the surfaceof the substrate, and the second terminal end optionally including asecond functional group selected to provide a SAM on the substrate thathas a desirable functionality, and/or a functionality that can bereacted to produce a desirable functionality, as further describedbelow. The spacer portion of the molecule may be selected to provide aparticular thickness of the resultant SAM, and/or to facilitate SAMformation. Although SAMs of the present invention may vary in thickness,e.g., as further described below, SAMs having a thickness of less thanabout 50 Angstroms, less than about 30 Angstroms or less than about 15Angstroms may be particularly useful in certain instances. Thesedimensions are generally dictated by the selection of the SAM-formingcompound and in particular the spacer portion thereof, and can bereadily selected and/or prepared by those of ordinary skill in the art.

The SAM-forming molecule, in some embodiments, may also include a spacerportion that interacts with neighboring molecules in the monolayer toform a relatively ordered array. The spacer functionality of theSAM-forming compound may connect a functional group able to bind orotherwise attach to the substrate with a functional group at a secondend of the molecule, as further described below. Alternately, a portionof the spacer may form the functional group. Any spacer that does notsubstantially and undesirably disrupt SAM packing is potentiallysuitable. The spacer may, in specific embodiments, be, for example,polar; non-polar; halogenated or, in particular, fluorinated; positivelycharged; negatively charged; or uncharged. As additional examples, asaturated or unsaturated, linear or branched alkyl, aryl, or otherhydrocarbon spacer may be used in certain embodiments of the SAM-formingcompound.

A variety of lengths of SAM-forming compounds can potentially beemployed in the present invention. If two or more different SAM-formingcompounds are used, it is sometimes advantageous that these species havesimilar lengths. However, in certain embodiments, for example when a twoor more step process is used, in which a first SAM is provided on asurface and at least a second SAM is provided on the surface, thevarious SAMs being continuous or noncontinuous, it may be advantageousin some circumstances to select molecular species for the formation ofthe various SAMs that have different lengths. For example, if the SAMinitially formed has a first molecular length and the SAM subsequentlyderivatized to the surface has a second molecular length greater thanthat of the first molecular length, a continuous SAM having a pluralityof “wells” may result. These wells are the result of the first SAM beingsurrounded by the second SAM having a longer chain length. Such wellsmay be advantageously fabricated according to certain embodiments, forexample, when it is desirable to add greater lateral stability toparticular biological materials, such as cells, which have been capturedin the wells. Such wells may also form the basis for reaction vessels.

Methods that can be used to form a SAM are well known and are describedin, for example, U.S. Pat. No. 5,620,850, which is hereby incorporatedby reference. See also, for example, Laibinis, P. E., Hickman, J.,Wrighton, M. S., Whitesides, G. M., Science, 245:845, 1989; Bain, C.,Evall, J., Whitesides, G. M., J. Am. Chem. Soc., 111:7155-7164, 1989;Bain, C., Whitesides, G. M., J. Am. Chem. Soc., 11 1:7164-7175, 1989,each of which is incorporated herein by reference. In some cases, theSAM can be made up of SAM-forming species that form SAMs on surfaces,and/or those species in combination with other species able toparticipate in a SAM. In some embodiments, some of the species thatparticipate in the SAM include a functionality or group able to bind,optionally covalently, to a surface, such as a thiol functionality whichwill chemisorb to a gold surface.

The SAM-forming compound may terminate in a second end, generallyopposite to the end bearing the functional group selected to bind to thesurface material. The second end can comprise any of a variety offunctionalities. For example, in one embodiment of the invention, atleast some of the SAM-forming molecules forming a SAM have a structure:

where | comprises a surface, X is an attachment moiety able tochemically bind a surface, Q comprises a photocleavable moiety, and R isa moiety connecting X and Q. As discussed above, the bond connecting Sto the substrate may be any bond capable of immobilizing the SAM-formingmolecule to the surface, for example, a chemisorption bond such as agold-sulfur bond. Q may also comprise other moieties, for example alkylmoieties, or functional moieties such as those described herein.

In one embodiment,

is not:

In one aspect of the invention, the compound to be attached to a surfaceof a substrate may have a structure:X—R-Q,where X is an attachment moiety able to chemically bind a surface, Qcomprises a photocleavable moiety, and R is a moiety connecting X and Q.An “attachment moiety” is a moiety of a molecule that can interact witha surface (e.g., through covalent binding) to attach the molecule to thesurface. An example of an attachment moiety is a thiol functionality(i.e., —SH), which may react covalently with a surface to produce asulfur-substrate bond, for example, a gold-sulfur bond if the surfacecomprises gold). Other examples of attachment moieties are disclosedherein.

Examples of photocleavable moieties are known to those of ordinary skillin the art. In one set of embodiments, a photocleavable moiety iscleaved from the compound upon exposure of the compound to lightcomprising a wavelength of at least about 250 nm, at least about 325 nm,or any other wavelength(s) disclosed herein. In some cases, thephotocleavable moiety may comprise an aromatic group, and in certaincases, the photocleavable moiety may comprise an aromatic group. In oneembodiment, the photocleavable moiety comprises a structure:

where each of Z¹, Z², Z³, Z⁴, Z⁵, and Z⁶ independently is one of —H, ahalogen, an alkyl such as methyl or ethyl, —OH, or an alkoxy such asmethoxy. As a non-limiting example, in one embodiment, at least two ofZ¹, Z², Z³, Z⁴, or Z⁵ independently is an alkoxy such as methoxy, withthe remainder of Z¹, Z², Z³, Z⁴, or Z⁵ being —H or an alkyl such asmethyl or ethyl, for example, as in a structure:

The above-described photocleavable moiety may be connected to the restof the molecule by an amide bond, e.g.,:

where Z⁶ is independently one of —H, a halogen, an alkyl, —OH, or analkoxy, and, upon photocleavage, the photocleavable moiety may no longerbe covalently attached to the rest of the molecule, i.e., uponphotocleavage, the photocleavable moiety forms a leaving group, forexample comprising a structure:

Q may also contain other moieties, for example, functional groups suchas those further described below, amino acids, additional alkylmoieties, ethylene glycol units, propylene glycol units, carbonyls,amide bonds, amines, alkoxys, halogens, etc. For instance, in oneembodiment, Q may have a structure:Q¹—R¹,where Q¹ is photocleavable and R¹ comprises an alkyl moiety.

In the discussions above, R is a moiety connecting X and Q. In somecases, R defines a series of atoms interconnected by covalent bondsbetween X and Q. R may include, for example, one or more alkyls,ethylene glycol units, propylene glycol units, carbonyls, alkoxys,halogens, etc. In some cases, R is not photocleavable.

In some embodiments, the systems and methods described herein use apolyfunctional alkanethiol that forms a SAM on a gold substrate and thatpresents two types of photocleavable bonds: an o-nitrobenzylamine-protecting group that cleaves on exposure to light at 365 nm and athiolate bond (Au‘S) that cleaves on exposure to light at 220 nm. Itshould be understood, however, that other similar embodiments havingpolyfunctional photocleavable bonds at the same or different wavelengthsmay be used for achieving the same or similar purposes and/or results.In addition, other suitable substrates for SAMs such as Ag, Pt, Pd,and/or Cu may be used. In cases where species other than alkanthiols areused to form one or multiple layers of molecules on the surface, such assilanes, other suitable substrates such as glass and silicon may beemployed.

In some embodiments, a photocleavable molecule that does not require theuse of scavengers, such as solution-phase scavengers, can be used. Forexample, photocleavable amine-protecting groups such as1-(3,4-(methylenedioxy)-6-nitrophenyl) ethylchloroformate (MeNPOC,(CH₃O)₂C₆H₂NO₂CH(CH₃)OCOCl), which cleaves quantitatively on photolysisusing near-UV light (365 nm) and regenerates the amines (FIG. 1A), canbe used. MeNPOC does not necessarily require the use of solution-phasescavengers. In some embodiments, a surface comprising MeNPOC may befurther modified: the amines generated by deprotection can be modifiedusing traditional solid-phase synthetic methods, or any other methodsfamiliar with those of ordinary skill in the art.

In another embodiment, photocleavable linkers, such as3-[5-(1-amino-ethyl)-2-methoxy-4-nitro-phenoxy]-propionic acid (NPOP,H₂NCH(CH₃)C₆H₂(OCH₃)O(CH₂)₃CO₂H), can be NPOP may permit the alkanethiolto include functional groups beyond the photosensitive group (FIG. 1B).The o-nitrobenzyl component can be modified to present another chemicalfunctionality, either before or after photopatterning. Thus, as anexample, a SAM that contains NPOP and that is exposed to light at 365 nmcan be converted to a SAM that terminates in primary amides, which canbe functionalized further (e.g., by reduction to amines with lithiumaluminum hydride).

Alkyl or aliphatic groups useful or potentially useful for practicingthe invention can contain any of a wide number of carbon atoms, forexample, between 1 and 30 carbon atoms, between 1 and 20 carbon atoms,between 1 and 15 carbon atoms, or between 1 and 10 carbon atoms. In someembodiments, the alkyl may have at least 2 carbon atoms, in otherembodiments at least 3 carbon atoms, in other embodiments at least 11carbon atoms, in other embodiments at least 13 carbon atoms, and inother embodiments at least 18 carbon atoms. In certain embodiments, thealkyl may have between 11 and 18 carbon atoms inclusive or between 13and 18 carbon atoms inclusive. In some cases, the alkyl may comprise achain of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 or morecarbon atoms. In one set of embodiments, the alkyl may be an undecyl, adodecyl, a tridecyl, a tetradecyl, a pentadecyl, a hexadecyl, aheptadecyl, or a octadecyl moiety. The carbon atoms may be arranged inany permissible configuration within the alkyl moiety, for example, as astraight chain or a branched chain (including multiple branches). Thealkyl moiety may contain only single bonds, or alternatively, maycontain one or more double or triple bonds within its structure, forexample, as in an alkene, an alkyne, an alkadiene, an alkadiyne, analkenyne, etc. The alkyl moiety may also contain one or moresubstituents in some embodiments. For example, in certain embodiments,the alkyl group may contain a halogen, an alkoxy (e.g., methoxy orethoxy), an amine (e.g., a primary, secondary, or tertiary amine), or ahydroxide as a substituent. If more than one substituent is present,then the substituents may be the same as or different from each other.In some cases, the carbon atoms may be interspersed with other atoms,for example, oxygen or nitrogen atoms. For example, the alkyl moiety maycomprise an amide bond, or one or more alkoxy moieties. In some cases,the alkyl may contain one or more rings (e.g., cycloalkyls, aromaticrings, etc.).

The term “halogen,” or equivalently, “halogen atom,” is given itsordinary meaning as used in the field of chemistry. The halogens includefluorine, chlorine, bromine, iodine, and astatine, and may have anycharge state and/or electronic configuration. In some cases, the halogenatoms include one or more of fluorine, chlorine, bromine, or iodine. Incertain embodiments, the halogen atoms found within the compositions ofthe invention are fluorine, chlorine, and bromine; fluorine andchlorine; chlorine and bromine, or a single type of halogen atom.

An “aromatic” moiety is given its ordinary meaning as used in the art,i.e., a moiety having at least one ring in which some electrons aredelocalized in the ring. For instance, the aromatic moiety may include abenzene moiety, a naphthalenyl moiety, an anthracenyl moiety, apyridinyl moiety, a furanyl moiety, etc. In one embodiment, the aromaticmoiety is a nitroaromatic moiety, i.e., an aromatic moiety comprising—NO₂.

In one set of embodiments, the alkyl may comprise polyethylene glycol(“PEG”) and/or polypropylene glycol (“PPG”) moieties, e.g., moietieshaving the general formula —(OCH₂CH₂)_(n)— or —(OCH₂CH₂CH₂)_(n)—,respectively, where n is any number of repeat units that gives theSAM-forming molecule, when the SAM-forming molecule is formed into a SAMon a surface, a desirable surface characteristic, such as cytophobicityor biophobicity, as those terms are further defined herein. The actualnumber of repeat units in the SAM-forming molecules utilized can bedetermined by those of ordinary skill in the art, depending on thespecific application, using routine experimentation. In certainembodiments, the functional group may include various combinations ofpolyethylene glycol and polypropylene glycol repeat units (includingblock and/or alternating combinations). In some cases, some or all ofthe polyethylene glycol and/or polypropylene glycol repeat units aresubstantially unmodified, i.e., the units have the general formula—(OCH₂CH₂)_(n)—OH and/or —(OCH₂CH₂CH₂)_(n)—OH, respectively. In certaincases each n can independently be between 1 and 20 inclusive, in certainembodiments between 1 and 10 inclusive, and in certain embodimentsbetween 1 and 8 inclusive. For instance, n may be at least 1, 2, 3, 4,5, 6, 7, 8, or 9.

In some cases, the molecule may comprise a functional group that confersa specific property to the SAM-forming molecule. That is, the compoundmay include a functionality that, when the compound forms a SAM on thesurface material, is able to confer upon the surface a specificproperty, such as an affinity for a particular entity or entities. Forexample, in certain non-limiting embodiments, the molecule can comprisea cytophilic moiety, a cytophobic moiety, a biophilic moiety, abiophobic moiety, a hydrophilic moiety, a hydrophobic moiety, achelating group, an antibody, a peptide or protein sequence, a nucleicacid sequence, an affinity tag (e.g., a member of a biotin/avidin orbiotin/streptavidin binding pair), or a moiety that selectively bindsvarious biological, biochemical, or other chemical species, etc.

In some embodiments, the molecule may include, for example, ionic,nonionic, polar, nonpolar, halogenated, alkyl, or aryl. A non-limiting,exemplary list of functional groups that Z could comprise include: —OH,—CONH—, —CONHCO—, —NH₂, —NH—, —COOH, —COOR, —CSNH—, —NO₂ ⁻—, —SO₂ ⁻—,—RCOR—, —RCSR—, —RSR, —ROR—, —PO₄ ⁻³, —OSO₃ ⁻², —COO⁻, —SOO⁻, —RSOR—,—CONR₂, —CH₃, —PO₃H⁻, −2-imidazole, —N(CH₃)₂, —NR₂, —PO₃H₂, —CN,—(CF₂)_(n)—CF₃ (where n=1-20 inclusive, and preferably 1-8, 3-6, or4-5), olefins, and the like. In addition to these, those mentioned aboveas forming part of the example SAM-forming molecules can also be usedmore generally. In the above list, R is hydrogen or an organic groupsuch as a hydrocarbon or an alkyl. As used herein, the term“hydrocarbon” includes alkyl, alkenyl, alkynyl, cycloalkyl, aryl,alkaryl, aralkyl, and the like. The hydrocarbon group may, for example,comprise methyl, propenyl, ethynyl, cyclohexyl, phenyl, tolyl, andbenzyl groups. The term “fluorinated hydrocarbon” is meant to refer tofluorinated derivatives of the above-described hydrocarbon groups. Instill another set of embodiments, the molecule may comprise a sulfonategroup (—SO₃ ⁻).

The molecules described herein may be synthesized using any methods thatare available to those of ordinary skill in the art. Some methods ofsynthesis are described briefly below; more detailed descriptions aredescribed in the Examples section. Synthesis of alkanethiols used forpatterning multiple, aligned SAMs is shown in FIG. 2; this figuredescribes the synthesis of the photocleavable alkanethiols. As anon-limiting example, to generate HS(CH₂)₁₁(EG)₂NPOC, a photocleavablethiol, a trityl-protected form of mercaptoundecanoic acid may be coupledto one amino group in H₂N(CH₂CH₂O)₂CH₂CH₂NH₂. The terminal amine of thiscompound can be allowed to react with MeNPOC; removal of the tritylprotecting group generated HS(CH₂)₁₁(EG)₂NPOC. FIG. 1 describes the useof this alkanethiol to pattern multiple, aligned SAMs.

As used herein, “affinity” refers to the degree and strength ofattraction between a first entity (e.g., a molecule) and a secondentity, which is reflective of the propensity of the first entity toattach to the second entity when the first and second entity are inproximity with each other. Thus, as used herein, a molecule (which maybe attached to a substrate) may have an affinity for an entity is ableto attach to and, in some cases, bind to the entity. The molecule may beable to attach to the entity by any suitable mechanism, for example, aphysical mechanism, such as physical adsorption, charge interactions,hydrophobic effects, van der Waals interactions, electrostaticattraction, magnetic attraction, molecular intercalation, etc., and/orvia bond-forming mechanisms, such as chemisorption, covalent bondformation, hydrogen bond formation, and the like. In one embodiment, themolecule is a binding partner. The term “binding partner” refers to amolecule that can undergo binding with a particular molecule. Biologicalbinding partners are examples. For example, Protein A is a bindingpartner of the biological molecule IgG, and vice versa.

In addition, in certain embodiments, functional groups comprising anaffinity tag may be employed. The term “affinity tag” is given itsordinary meaning in the art. An affinity tag is any biological orchemical material that can readily be attached to a target biological orchemical material. Affinity tags may be attached to a target biologicalor chemical molecule by any suitable method known in the art. Forexample, in some embodiments, the affinity tag may be attached to atarget nucleic acid sequence using a nucleic acid sequence complementaryto the target nucleic acid sequence. As another example, an affinity tagsuch as biotin may be chemically coupled, for instance covalently, to atarget protein or peptide, by allowing binding of biotin to an avidinand/or streptavidin moiety fastened with respect to the target proteinor peptide.

The term “biological binding” refers to the interaction between acorresponding pair of molecules that exhibit mutual affinity or bindingcapacity, typically specific or non-specific binding or interaction,including biochemical, physiological, and/or pharmaceuticalinteractions. Biological binding defines a type of interaction thatoccurs between pairs of molecules including proteins, nucleic acids,glycoproteins, carbohydrates, hormones and the like. Specific examplesinclude antibody/antigen, antibody/hapten, enzyme/substrate,enzyme/inhibitor, enzyme/cofactor, binding protein/substrate, carrierprotein/substrate, lectin/carbohydrate, receptor/hormone,receptor/effector, complementary strands of nucleic acid,protein/nucleic acid repressor/inducer, ligand/cell surface receptor,virus/ligand, etc.

In some of the embodiments described herein involving SAMs formed of SAMforming molecules having a functional group, the SAMs may be formed thatcomprise molecules having a particular functional group, the SAMs may beformed that consist essentially of molecules having a particularfunctional group, or the SAMs may be formed that consist of moleculeshaving a particular functional group. In certain embodiments, SAMs maybe formed comprising a plurality of molecules providing a plurality ofdifferent functional groups.

In one set of embodiments, the functional group may be chosen from awide variety of compounds or fragments thereof which will render the SAMgenerally or specifically “biophilic” as this term is defined below.“Generally biophilic” functional groups are those that would have atendency to promote the binding, adherence, or adsorption of biologicalmaterials such as, for example, intact cells (e.g., “cytophilic”functional groups), fractionated cells, cellular organelles, proteins,lipids, polysaccharides, simple carbohydrates, complex carbohydrates,nucleic acids, etc. Generally biophilic functional groups can includehydrophobic groups or alkyl groups with charged moieties such as COO⁻,PO₃H⁻, or 2-imidazolo groups, and/or compounds or fragments of compoundssuch as extracellular matrix proteins, fibronectin, collagen, laminin,serum albumin, polygalactose, sialic acid, one or more amino acids, e.g.peptide sequences such as RGD or GRGD, antibodies, and various lectinbinding sugars. “Specifically biophilic” functional groups are thosethat selectively or preferentially bind, adhere or adsorb a specifictype or types of biological material so as, for example, to identifyand/or isolate the specific material from a mixture of materials.Specifically biophilic materials include antibodies or fragments ofantibodies and their antigens, cell surface receptors and their ligands,nucleic acid sequences and many others that are known to those ofordinary skill in the art. The choice of an appropriate biophilicfunctional group depends on considerations of the biological materialsought to be bound, the affinity of the binding required, availability,ease of use, effect on the ability of the SAM-forming compound toeffectively form a SAM, and cost. Such selection is within theknowledge, ability and discretion of one of ordinary skill in the art.

In another set of embodiments, the functional group may be chosen from awide variety of compounds or fragments thereof which will render theSAMs “cytophilic,” that is, adapted to promote cell attachment.Molecular entities creating cytophilic surfaces are well known to thoseof ordinary skill in the art and include antigens, antibodies, celladhesion molecules, extracellular matrix molecules such as laminin,fibronectin, synthetic peptides, carbohydrates, peptide sequences suchas RGD, and the like.

In another set of embodiments, the functional group may be chosen from awide variety of compounds or fragments thereof which will render the SAM“biophobic” as that term is defined below. “Biophobic” SAMs are thosewith a generally low affinity for binding, adhering, or adsorbingbiological materials such as, for example, intact cells, fractionatedcells, cellular organelles, proteins, lipids, polysaccharides, simplecarbohydrates, complex carbohydrates, and/or nucleic acids. Biophobicfunctional groups can include polar but uncharged groups includingunsaturated hydrocarbons. In certain embodiments, biophobic functionalgroups can include hydrophilic groups, such as the polyethylene glycoland/or polypropylene glycol moieties previously discussed.

In yet another set of embodiments, the functional groups may be chosenfrom a wide variety of compounds or fragments thereof which will renderthe SAM “cytophobic,” i.e., such that the SAM has a generally lowaffinity for binding, adhering, or adsorbing cells. Molecular entitiesknown to create cytophobic surfaces can be selected by those of ordinaryskill in the art and include, for example, but not limited to, thosegroups mentioned above as being biophobic, such as uncharged functionalgroups such as unsaturated hydrocarbons, or polyethylene glycol groups,etc.

In certain embodiments, the functional groups may be chosen to renderthe SAM-coated surface hydrophobic and/or hydrophilic. As used herein,the terms “hydrophobic” and “hydrophilic” are given their ordinarymeaning as used in the art. In certain cases, a hydrophilic surface mayalso be cytophobic and/or biophobic, while a hydrophobic surface mayalso be, in some cases, cytophilic and/or biophilic. The degree ofhydrophilicity of a hydrophilic and/or a hydrophobic surface can bereadily determined and controlled via proper selection of SAMs bearingparticular expressed functional groups as determined through no morethan routine experimentation by those of ordinary skill in the art, forexample, by using contact angle measurements, determining the water/oilpartition coefficient of the molecules and/or the functional groups thatcomprise the SAM, etc. In some cases, the terms “hydrophobic” and“hydrophilic” are defined relative to each other, where the hydrophilicentity has a greater affinity to water than does the hydrophobic entity.

Thus, in one set of embodiments, a photocleavable alkanethiol may beused that contains one or more functional groups. One non-limitingexample is a photocleavable alkanethiol, HS(CH₂)₁₁EG₆NPOP(GRGD),containing a photocleavable linker that allows functional groups to beadded beyond the photocleavable group, NPOP, for example, a peptidesequence such as Gly-Arg-Gly-Asp (GRGD) (e.g., which may be synthesizedon a Wang resin). In this particular example, the photocleavable linkercan be coupled to this peptide, and then a trityl-protected alkanethiolcan be coupled to the photocleavable linker on the solid support. Theremoval of all protecting groups (except the photocleavable linker)produced HS(CH₂)₁₁EG₆NPOP(GRGD). FIG. 1 also shows the use of thisalkanethiol to pattern multiple, aligned SAMs.

As is apparent from the description, the use of self-assembledmonolayers that expose a variety of chemical functionalities on surfacesaccording to the invention is a common feature of many embodiments ofthe invention. In addition to the extensive and enabling description ofvarious functional groups useful or potentially useful as exposedfunctionalities on SAMs utilized for particular purposes, additionaldisclosure related to hydrophobic, hydrophilic, biophobic, biophilic,cytophobic, cytophilic, and other functionalities incorporated into SAMsand/or SAM-forming molecules can be found in the following references,all incorporated herein by reference: U.S. Provisional PatentApplication Ser. No. 60/443,446, filed Jan. 29, 2003, entitled“Alteration of Surface Affinities,” by Jiang, et al.; U.S. Pat. No.6,472,148, entitled “Molecular Recognition at Surfaces Derivatized WithSelf-Assembled Monolayers,” by Bamdad, et al.; U.S. Pat. No. 6,368,838,entitled “Adhering Cells to Cytophilic Islands Separated by CytophobicRegions to Form Patterns and Manipulate Cells,” by Singhvi et al.; U.S.Pat. No. 6,355,198, entitled “Method of Forming Articles IncludingWaveguides via Capillary Micromolding and Microtransfer Molding,” by Kimet al.; U.S. Pat. No. 6,180,239, entitled “Microcontact Printing onSurfaces and Derivative Articles,” by Whitesides, et al.; U.S. Pat. No.5,976,826, entitled “Device Containing Cytophilic Islands that AdhereCells Separated by Cytophobic Regions,” by Singhvi, et al.; U.S. Pat.No. 5,900,160, entitled “Methods of Etching Articles via MicrocontactPrinting,” by Whitesides, et al.; U.S. Pat. No. 5,776,748, entitled“Methods of Formation of Microstamped Patterns on Plate for Adhesion ofCells and Other Biological Materials, Devices and Uses Therefor,” bySinghvi, et al.; U.S. Pat. No. 5,512,131, entitled “Formation ofMicrostamped Patterns on Surfaces and Derivative Articles,” by Kumar, etal.; U.S. Pat. No. 5,079,600, entitled “High Resolution Patterning onSolid Substrates,” by Schnur, et al.; U.S. patent aplication Ser. No.09/808,745, entitled “Cell Patterning Technique,” by Ostuni, et al.;International Pat. Apl. Pub. No. WO 02/06407, entitled “Surfaces thatResist the Adsorption of Biological Species,” by Whitesides, et al.;International Pat. Apl. Pub. No. WO 01/89788, entitled “Patterning ofSurfaces Utilizing Microphilitic Stamps including Three-DimensionallyArrayed Channel Networks,” by Whitesides, et al.; Kleinfeld, et al.,“Controlled outgrowth of dissociated neurons on patterned substrates,”Journal of Neuroscience, 8(11):4098, 1988; Westermark, B., “GrowthControl in Miniclones of Human Glial Cells”, Experimental Cell Research,111:295-299, 1978; Britland, S., et al., “Micropatterned SubstratumAdhesiveness: a Model for Morphogenetic Cues Controlling Cell Behavior,”Experimental Cell Research, 198:124-129, 1992; Singhvi, R., et al.,“Engineering Cell Shape and Function,” Science, 264:696, 1994; Lopez, G.P., et al., “Convenient Methods of Patterning the Adhesion of MammalianCells to Surfaces Using Self-Assembled Monolayers of Alkanethiolates onGold,” Journal of the American Chemical Society, 115:5877-5878, 1993;U.S. Provisional Patent Application Ser. No. 60/443,466, filed Jan. 29,2003, entitled “Alteration of Surface Affinities,” by Jiang, et al.; andInternational Patent Application No. PCT/US2004/002498, filed Jan. 29,2004, entitled “Alteration of Surface Affinities,” by Jiang, et al.

An enormous variety of patterns may be produced and a multiplicity ofSAMs may be employed to create patterns of one or more types of cells.As discussed previously, the SAMs employed for embodiments involvingcell binding and manipulation may be either generally or specificallybiophilic/cytophilic or biophobic/cytophobic as applied (or certainsurfaces may contain certain regions with generally biophilic/cytophilicor biophobic/cytophobic SAMs, while other regions contain specificallybiophilic/cytophilic or biophobic/cytophobic SAMs). In some cases, theSAMs may be modified after SAM formation to become generally orspecifically biophilic/cytophilic or biophobic/cytophobic by chemicalmodification of exposed functional groups. For example, when severalSAMs are present in a pattern but only one is cytophilic, a first typeof cell may be adhered to the cytophilic SAM and then a cytophobic SAMmay be chemically modified in situ so as to become cytophilic. In somecases, a second cell type may then be adhered to the newly cytophilicSAM and this process can be repeated to create a complex pattern ofdifferent cell types. Similarly, if several SAMs are present in apattern but only one is biophilic, a first type of biological entity maybe adhered to the biophilic SAM and then a biophobic SAM may bechemically modified in situ so as to become biophilic. A secondbiological entity, may then be adhered to the newly biophilic SAM insome cases, and this process can be repeated to create a complexpattern.

In another aspect of the present invention, SAM-patterned substrates areprovided which may be used to bind or adsorb proteins and/or otherbiological entities (e.g., cells) in specific and predeterminedpatterns. As is known to those of ordinary skill in the art, phenomenaassociated with the adsorption of proteins to solid synthetic materialsare important in many areas of biotechnology including, for example,production, storage and delivery of pharmaceutical proteins,purification of proteins by chromatography, design of biosensors andprosthetic devices, and production of supports for attached tissueculture (see, for example, ACS Symposium Series 343, T. A. Horbett andJ. L. Brash, Eds., Am. Chem. Soc., Washington, DC., 1987; J. D. Andrade,Surface and Interfacial Aspects of Biomedical Polymers: ProteinAdsorption, Plenum Press, N.Y., 1985; Materials Research SocietyProceedings 252, L. G. Cima and E. Ron, Eds., Mat. Res. Soc.,Pittsburgh, Pa., 1992). A number of researchers have demonstrated theformation of patterns of proteins (see, for example, A. S. Lea, et al.,Langmuir 8-68-73, 1992). These have often relied on photolithography tocreate the patterns (see, for example, S. K. Bhatia, et al., J. Am.Chem. Soc., 114:4432-4433, 1992; S. K. Bhatia, et al., Anal. Biochem.,208:197-205, 1993). The present invention provides for relativelyinexpensive and efficient patterning of proteins and manipulation of theaffinity of a substrate for proteins via utilization of a non-chemicalforce-creating field and/or forces such as an electric field, withfeatures of the pattern as small as 0.1-1 microns in some cases.

In similar embodiments, a substrate can be created with patterned SAMsthereon as described previously. Depending upon the desired application,the pattern may include islands or parallel rows of SAMs with differentproperties. One portion of the substrate may be biophilic/cytophilic andthe other may be biophobic/cytophobic as applied, or they may bemodified so as to become biophilic/cytophilic or biophobic/cytophobicsubsequent to SAM formation, i.e., through exposure to an electric fieldas described. In a particular embodiment, a substrate surface mayinclude a biophilic region of SAMs and a biophobic region of SAMs and,subsequent to binding a protein or proteins to the biophilic SAM, thebiophobic region may be modified so as to become biophilic, i.e.,through biophilic SAM removal via exposure to an electric field. In thisway, a pattern of two or more protein groups may be created. Similarly,patterns of more than two SAMs may be used to create more complicatedpatterns of proteins in accordance with the present invention. Theextent of binding of the proteins to the substrate may also becontrolled and/or changed by the use of an electric field (or othernon-chemical force-creating field). For example, proteins attached toSAMs present in certain portions of the substrate may be selectivelydetached by application of an electric field to those portions, in somecases without creating an electric field capable of SAM detachment inother portions of the substrate. In many embodiments, the electric fieldmay be applied to the substrate to detach SAM-forming molecules asprovided according to the invention even in the presence of animal serum(e.g., calf serum or human serum), or in the presence of other,undefined media (i.e., media in which the exact chemical composition isnot known), whereas typical prior art techniques for electricfield-mediated alteration of SAMs on surfaces do not have this capacity(see, e.g., Yousaf, et al, Angew. Chem. Int. Ed., 40:1093, 2001).

In certain embodiments, a substrate with patterned proteins may beprepared as described above and cells may then be allowed to adhere tothe patterned proteins to form a substrate having patterned cellsthereon; In some embodiments, the proteins may include extracellularmatrix proteins or ligands for receptors such as collagen, fibronectinor laminin; or specific cell receptors such as integrins. In certainembodiments, the patterned protein can mediate the cell adhesionbehavior of the patterned cells. In yet another embodiment, a patternedsubstrate of biophilic and biophobic SAMs may be created and a widevariety of non-protein compounds may first be adhered to the pattern tomediate cell binding. Such compounds include but are not limited tosialic acid, lectins, polygalactose and other carbohydrates.

The surface material of the substrate may comprise the entire substrateonto which the patterned SAMs of the present invention are bonded orotherwise attached, or may be a thin film deposited upon an article.Where a separate substrate is used, it may comprise any of a widevariety of biological, non-biological, organic, or inorganic materials,or a combination of any of these existing as particles, strands,precipitates, gels, sheets, tubing, spheres, containers, capillaries,pads, slices, films, slides, plates, etc. In certain embodiments, thesubstrate of the present invention is substantially planar, although itneed not be according to other embodiments. The substrate may be formedof a conductive material, a semiconducting material, and/ornon-conducting material, and may comprise, for example, alumina, plasticor other organic polymers including acrylonitrile-butadine-styrenecopolymers, polysulfone, metals and/or any of the above materialsdescribed with respect to the surface material of the present invention.The substrate may additionally include a bonding layer, for example athin titanium film, to promote adhesion between the surface material andthe substrate.

The surface material, for embodiments involving coated substrates, isgenerally of a thickness on the order of 500 microns, but may besubstantially thicker or may be substantially thinner. For example, whena substrate as a base material is employed, the surface material mayhave a thickness of less than about 100 nanometers, less than about 10nanometers, or even less than about 6 nanometers. When a thin film ofsurface material is employed, and a transparent substrate supports thesurface material, a transparent base support for a SAM can result, andthis may be advantageous in standard light or electron microscopic orspectrophotometric detection or analysis of any biological materialinteracting with a SAM on the surface material.

In certain sets of embodiments, SAMs formed on a substrate surface maybe modified after formation for a variety of purposes. For example, aSAM-forming compound on a substrate may have a functionality including aprotecting group which may be removed to effect further modification ofthe SAM (i.e., to produce a specific surface chemistry). For instance, aphotoremovable protecting group may be used, where the group isadvantageously selected such that it may be removed without disturbanceof the SAM of which it is a part. For example, a protective group may beselected from a wide variety of positive light-reactive groups, forexample, nitroaromatic compounds such as o-nitrobenzyl derivatives orbenzylsulfonyl. A variety of photoprotecting groups can be used toprotect different functional groups, e.g., alcohols, carboxylic acids,thiols, etc. Photoremovable protective groups can be readily selected bythose of ordinary skill in the art and are described in, for example,U.S. Pat. No. 5,143,854, issued Sep. 1, 1992; Patchornik, J. Am. Chem.Soc., 92:6333, 1970; or Amit, et al., J. Org. Chem., 39:192, 1974, allof which are incorporated herein by reference. Alternatively, a reactivegroup may be provided on an exposed portion of a SAM that may beactivated or deactivated by electron beam lithography, x-raylithography, or any other suitable type of radiation exposure. Suchprotections and deprotections of functional groups may aid in chemicalor physical modification of an existing surface-bound SAM, for examplein lengthening existing molecular species forming the SAM, for example,as described in U.S. Pat. No. 5,143,857, incorporated herein byreference.

As a specific example, when only a subset of cells in a sample aredesired to be immobilized to an article of the invention, for example,the white blood cells in a blood sample containing both red and whiteblood cells, a specifically biophilic SAM may be chosen that willselectively bind the cells of interest and, subsequent to binding, theextraneous cells may be washed away. Given a particular set or subset ofcells to be studied, the choice of a biophilic SAM specific to thosecells is within the ability of one of ordinary skill in the art and,given the disclosures herein, one of ordinary skill in the art isenabled to produce appropriate patterned biophilic SAMs specific forthose cells.

Many methods may be used to apply and attach the SAM-forming moleculesto a substrate surface. For example, the SAM-forming molecules may beapplied to the substrate by stamping or micropatterning techniques,organic synthesis techniques, and the like. A variety of suitablemethods to attach the SAM to the substrate are known in the art and maybe chosen by one of ordinary skill in the art to suit a particularpurpose.

For example, in one set of embodiments, the SAM-forming molecules may bepatterned on the substrate using a stamp in a “printing” process inwhich the “ink” consists of a solution including a SAM-forming compoundcapable of attaching to a surface to form a SAM. The ink is applied tothe surface of a substrate using the stamp and deposits a SAM on thesubstrate in a pattern determined by the pattern on the stamp. Thesubstrate may be stamped repeatedly with the same or different stamps invarious orientations and with the same or different SAM-formingsolutions. In addition, after stamping, portions of the substrate whichremain uncovered by SAMs may optionally be derivatized using anysuitable technique known in the art, for example, exposure of theuncovered portions to another solution containing a SAM-formingcompound. The SAM-forming or derivatizing solutions can be chosen suchthat the regions of the finished substrate defined by the patternsdiffer from each other in their ability to bind to materials such asbiological or biochemical materials (e.g., proteins, drugs, cells,etc.). As one example, cytophobic SAM-forming compounds may be patternedon a cytophilic substrate to create a pattern of cytophobic SAMs andcytophilic regions not containing SAMs (or, alternatively, containingcytophilic SAMs), such that certain cells applied to the substrate canbind to the cytophilic regions, but are unable to bind to regionscontaining the SAMs; thereafter, application of a suitable electricfield to the substrate, or to portions of the substrate, may detach theSAMs from the substrate or those in those portions subjected to thefield, permitting the cells to then migrate into those portions wherethe SAMs have been detached.

In certain embodiments, the stamp described above may be formed via amolding process. The mold used to form the stamp may be a commerciallyavailable item such as a transmission electron microscopy grid or anyother corrugated material possessing a pattern which is desired to bereproduced on the stamp, or a mold especially prepared by any of avariety of methods known in the art. The stamp may be produced bycasting a material, e.g., a polymer such as a silicon polymer (e.g.,polydimethylsiloxane) onto a mold having the desired pattern. Varioustechniques for forming stamps for patterning SAMs are known in the artand several are described in detail in, for example, U.S. Pat. No.6,368,838, by Singhvi, et al., entitled “Adhering Cells to CytophilicIslands Separated by Cytophobic Regions to form Patterns and ManipulateCells,” hereby incorporated by reference, to which the reader isreferred to for more details.

As mentioned above, in some embodiments, after a desired SAM pattern hasbeen formed on the substrate by stamping, the portion of the substratewhich is bare or not covered by the stamped SAM may be further reactedor otherwise processed, for example, to add chemical functionalitythereto, or to add one or more additional regions containing SAMs. Forexample, the portion of the substrate which is not covered by thestamped SAM may, in some cases, be derivatized by exposing it to asecond or “filling” solution with characteristics differing from thefirst solution which was used as the ink for forming the initial stampedpattern. This exposure may be accomplished using stamping techniquessimilar to those previously described, by dipping the substrate in abath of solution, by pouring the solution onto the substrate, or by anyother convenient method which preferably does not disrupt the patternedSAM. The second solution in certain embodiments may form a SAM over thesurface of the plate which is not already covered by the patterned SAMof the ink. That is, the second of filling solution may contain a secondSAM-forming compound which will form a second or “filling” SAM on thebare portions of the substrate. The result of such an embodiment can bea plate essentially completely covered by complementary patterns of twoor more SAMs of differing properties. As an example, two SAM-formingcompounds able bind different cell types may be patterned on a substratesuch that one SAM region is able to bind a first cell type and a secondSAM region separate from the first region is able to bind a second celltype; application of an electric field to the substrate may then causeselective detachment of one of the SAMs, and consequently, selectivedetachment of only one of the cell types.

Of course, it is not necessary in all embodiments to derivatize orotherwise react or coat any bare portions of the surface remaining afterforming patterned SAMs. Depending upon the surface used, the baresurface may have the desired biophilic or biophobic characteristics and,thus, any additional steps may be omitted. For example, when it isdesired that cells adhere to a portion of a surface, exposure of thebare surface to a medium containing serum may be sufficient tofacilitate binding of the cells.

In certain embodiments, the substrate may be patterned such that one ormore regions on the surface are able to bind cells and/or otherentities, while a second region on the surface is unable to bind thecells and/or other entities; exposure of the second region to anelectric field may then change the affinity of the second region (e.g.,by detaching SAM-forming molecules at their point of attachment to thesurface) so as to allow the second region to then bind the cells and/orthe other entities. The regions may be distributed in any suitablepattern on the surface, for example, half of the substrate may becytophilic and/or biophilic, while the other half of the substrate maybe cytophobic and/or biophobic. In another embodiment, the two or moreregions may be distributed such that one or more regions forms channelsor isolated islands within another region. As used herein, an “island”is a contiguous region adapted to bind to a particular entity or classof similar entities, such as cells and/or other entities generally, or aparticular type of cell or type of entities.

Multiple, aligned patterns of SAMs may be used to pattern multiple typesof cells and for studying cell-cell signaling (e.g., where one cell typeis separated from the other).

In one set of embodiments, a method of using certain articles andsubstrates of the invention for assaying the effects of varioustreatments and compounds such as drugs on cells is provided. In oneembodiment, the invention provides the capability to assay the effectsof various treatments or compounds on various cells adhered to asubstrate. As one example, once a suspension of cells-has been appliedto a substrate containing cytophilic regions and SAM-coated cytophobicregions, a period of time is allowed to elapse in order to allow thecells to bind to the cytophilic regions of the substrate. Excess fluidincluding unbound cells may then be washed away. The cells may then besubjected to a treatment or exposed to a compound in situ or, in somesituations, the cells may be pre-treated before being introduced to thesubstrate for attachment. The effects of the treatment or compound onthe cells may then be individually assayed in a manner appropriate tothe cell type and the treatment or compound being studied, for example,using analytical techniques such as those previously described. Forexample, cells may be removed from a surface by exposing at least aportion of the surface to light, thereby cleaving at least a portion ofthe molecules forming a SAM.

In one set of embodiments, a cell motility assay of the invention can beautomated. For example, in one embodiment, exposure of the substrate tothe electric field, and/or detection of cell positions and/or migrationbehavior on the substrate may be automated, for example, with a computeror a mechanical system.

In some cases, a detector unit able to detect cell positions and/or cellmigration behavior may include a multiplicity of individual detectors inan array corresponding and addressable to individual positions, regions,and/or islands on the substrate, as described above. For example, thedetector may be a CCD camera or a semiconductor chip. In certain cases,the effect of a treatment or compound on many cells and/or cell typesmay be assessed simultaneously, with minimal user involvement.

In certain cases, the above-described embodiments, which allow forplating of cells at high densities, can be employed for high throughputtests of potentially useful treatments including pharmacological ortoxicological compounds. In particular, the present invention providesassays which allow qualitative and quantitative changes in cell behavioror position in response to a change in the area over which they arepermitted to adhere, to be determined and/or measured as a function ofexposure to a given treatment or compound. In other embodiments, theinventive techniques can be utilized to assay various aspects related tothe proliferation, differentiation, orientation, spreading, motilityand/or migration of cells.

The following examples are intended to illustrate certain embodiments ofthe present invention, but do not exemplify the full scope of theinvention.

EXAMPLE 1 Syntheses of Alkanethiols Used for Patterning Multiple,Aligned SAMs

This example describes procedures for synthesizing certainphotocleavable alkanethiols that were used in the formation of SAMs on agold surface. As would be understood by those of ordinary skill in theart, similar techniques as described below and/or other procedures forsynthesizing known in the art could be employed to make various otherphotocleavable alkanethiols within the scope of the invention.Similarly, modifications of the techniques below and/or use of a varietyof other know techniques could be employed by those of ordinary skill inthe art to synthesize other molecules, such as SAM-forming molecules,having a moiety able to react with and bind to a surface of an articleof the invention (e.g. in certain embodiments a silane moiety or thiolmoiety), and a photocleavable moiety(s).

FIG. 2 describes the synthesis of photocleavable alkanethiols. Briefly,a trityl-protected form of mercaptoundecanoic acid was coupled to oneamino group in H₂N(CH₂CH₂O)₂CH₂CH₂NH₂. The terminal amine of thiscompound was allowed to react with MeNPOC; removal of the tritylprotecting group generated HS(CH₂)₁₁(EG)₂NPOC (5). FIG. 1 describes theuse of this alkanethiol to pattern multiple, aligned SAMs.

A second embodiment of a photocleavable alkanethiol,HS(CH₂)₁₁EG₆NPOP(GRGD), contained a photocleavable linker that allowedfunctional groups to be added beyond the photocleavable group, NPOP. Wesynthesized the peptide sequence Gly-Arg-Gly-Asp (GRGD) on a Wang resin,(Fields, G. B.; Noble, R. L. Int. J. Pept. Protein Res. 1990, 35,161-214) coupled the photocleavable linker to this peptide, and thencoupled a trityl-protected alkanethiol to the photocleavable linker onthe solid support. The removal of all protecting groups (except thephotocleavable linker) produced HS(CH₂)₁₁EG₆NPOP(GRGD) (8). FIG. 1 alsoshows the use of this alkanethiol to pattern multiple, aligned SAMs.

Materials. All chemicals were purchased from Aldrich (St. Louis, Mo.)unless stated otherwise. MeNPOC was obtained from Cambridge MajorLaboratories (Germantown, Wis.). Anti-dinitrophenol delipidized rabbitanti-serum (anti-DNP rIgG), monoclonal anti-biotin mouse immunoglobulinG (anti-biotin mIgG), monoclonal anti-bovine serum albumin mouse IgG(anti-BSA mIgG), anti-bovine serum albumin rabbit IgG (anti-BSA rIgG),phosphate-buffered saline (PBS), and fibrinogen were purchased fromSigma (St. Louis, Mo.). Texas Red labeled anti-rabbit donkey IgG(TR-anti-rabbit IgG) was obtained from Amersham Biosciences (Newark,N.J.). Alexa Fluor 488 labeled anti-mouse IgG (AF488-anti-mouse IgG) wasobtained from Molecular Probes (Eugene, Oreg.). The quantities ofantibodies used are quoted as a ratio relative to the stockconcentration acquired commercially, for example, 1:10 implies a 1:10dilution in blocking buffer (0.05% Tween (w/v) in PBS) of theconcentration provided by the supplier was used. H-1000 mounting mediumfor fluorescence was obtained from Vector Laboratories (Burlingame,Calif.).

Analytical HPLC was run on a Varian instrument (Walnut Creek, Calif.)with a Microsorb C18 column (5 μm, 4.6×250 mm) using a linear gradientof water with 0.1 % trifluoroacetic acid (TFA) (A) followed byacetonitrile containing 0.08% TFA (B), at a flow rate of 1.2 mL/min (UVdetection at 214 nm). Preparative reverse-phase HPLC was performed usinga Varian apparatus on a C18 column (5 μm, 10×250 mm) at a flow rate of 6mL/min (UV detection at 214 nm). Amino acids and derivatives wereobtained from Novabiochem (San Diego, Calif.).4-{4-[1-(Fmoc-amino)ethyl]-2-methoxy-5-nitrophenoxy}butyric acid waspurchased from Advanced Chemtech (Louisville, Ky.). Mass spectra oforganic molecules (not SAMs) were obtained by MALDI-TOF massspectrometry on a Voyager-DE PRO (PerSeptive Biosystems, Foster City,Calif.). MALDI-TOF mass spectra of SAMs were analyzed on a Voyager-DEBiospectroscopy mass spectrometer using 2,4,6-trihydroxyacetophenone (5μL of a 10 mg/mL solution in acetone) as a matrix. SPR experiments wereperformed using a Biacore 1000 SPR instrument (Piscataway, N.J.).Solutions of fibrinogen (1 mg/mL, PBS buffer) were used in all SPRexperiments, and solutions were filtered through 0.2-μm poly(vinylidenefluoride) filters immediately before use. Fluorescence images wererecorded using an ORCA-ER Hamamatsu charge coupled device camera mountedon a DMIRB Leica inverted fluorescence microscope (DSC Optical Services;Newton, Mass.). An AB-M Mask Aligner (AB-M Inc.; San Jose, Calif.) wasused as a light source for 220 and 365 nm wavelengths. Mirrors thatselect for each of these wavelengths were used separately during theexperiments.

The alkanethiols(2-{2-[2-(11-mercapto-undecanoylamino)-ethoxy]-ethoxy}-ethyl)-carbamicacid 1-(4,5-dimethoxy-2-nitro-phenyl)-ethyl ester (HS(CH₂)₁₁(EG)₂NPOC)and 11-mercapto-undecanoic acid[2-(2-{2-[2-(2,4-dinitro-pheylamino)-acetylamino]-ethoxy}-ethoxy)-ethyl]-amide(HS(CH₂)₁₁(EG)₂DNP) were prepared according to the reaction scheme shownin FIG. 2A. All reactions involving MeNPOC and NPOP were carried out inaluminum-foil-coated flasks to exclude light during reactions.

Synthesis of 11-Tritylsulfanyl-undecanoic Acid (2). To a solution oftrityl chloride (4.6 g, 17 mmol) and diisopropylethylamine (DIEA, 4.2 g,33 mmol) in toluene (50 mL) was added 11-mercaptoundecanoic acid, 1 (6.0g, 14 mmol), and the solution was stirred at room temperature for 3 h.The solution was evaporated, and the product separated betweendichloromethane and water. The organic phase was washed with water(2×100 mL), dried (MgSO₄), filtered, and concentrated to yield crude 2(6.3 g, 13.6 mmol, 97%). ¹H NMR (CDCl₃, 500 MHz): δ1.14-1.42 (br m,14H), 1.59-1.68 (br t, 2H), 2.06-2.09 (br m, 2H), 2.36-=2.40 (t, 2H),7.19-7.23 (m, 6H), 7.26-7.29 (m, 9H).

11-Tritylsulfanyl-undecanoic Acid{2-[2-(2-Aminoethoxy)ethoxyl-ethyl}-amide (3). To a solution ofN-hydroxysuccinimide (0.26 g, 2.3 mmol) and a catalytic amount of4-(dimethylamino)pyridine in anhydrous dichloromethane (50 mL) was addedcrude 2 (1.03 g, 2.2 mmol). Dicyclohexylcarbodiimide (0.46 g, 2.2 mmol)was added to the solution. The reaction was cooled for the first hour at5° C. and left to react at room temperature overnight. The solution wasdiluted with dichloromethane, filtered to remove dicyclohexylurea, andevaporated to dryness to yield the active ester of 2 (1.1 g, 2 mmol). Toa stirred solution of this active ester (1.1 g, 2 mmol) indichloromethane (50 mL) was added 2,2′-(ethylenedioxy)bisdiethylamine(5.1 g, 34 mmol) over a period of 30 min. The reaction was left at roomtemperature for 12 h. The solution was filtered, washed with water(3×200 mL), dried (MgSO₄), and concentrated to yield 3 (1.25 g, 2.1mmol, 95%). ¹H NMR (CDCl₃, 500 MHz): δ1.24-11.42 (br m, 14H), 1.59-1.68(br t, 2H), 2.06-2.09 (m, 2H), 2.78-2.85 (br t, 2H), 3.38-3.42 (m, 4H),3.46-3.51 (m, 4H), 3.58-3.63 (s, 4H), 7.19-7.23 (m, 6H), 7.26-7.29 (m,9H). C₃₆H₅₀N₂O₃S (590.35): m/z 591.1[M+H^(+]+. ()2-{2-[2-(11-Tritylsulfanyl-undecanoylamino)-ethoxy]-ethoxy}-ethyl)-carbamicAcid 1-(4,5-Dimethoxy-2-nitro-phenyl)-ethyl Ester (4). To a stirredsolution of 3 (1.03 g, 1.74 mmol) and DIEA (0.26 g, 2.0 mmol) indichloromethane (50 mL) was added MeNPOC (0.59 g, 2.0 mmol) over aperiod of 30 min. The reaction was cooled for the first hour at 5° C.and then left to react at room temperature overnight. The solution waswashed with 0.01 M HCl (1×100 mL), 0.2 M NaOH (1×100 mL), and saturatedaqueous NaCl solution (1×100 mL). The solution was dried (MgSO₄) andevaporated to dryness. The crude compound was chromatographed(SiO₂/EtOAc→MeOH) to yield 1.2 g (1.4 mmol, 82%) of 4 as a yellow oil.¹H NMR (CDCl₃, 500 MHz): δ1.24-1.42 (br m, 10H), 1.59-1.71 (br m, 4H),1.82-1.93 (br t, 2H), 2.02-2.11 (br m, 2H), 2.78-2.85 (br t, 2H),3.38-3.42 (m, 4H), 3.46-3.51 (m, 4H), 3.58-3.63 (s, 4H), 3.63-3.66 (s,3H), 3.66-3.69 (s, 3H), 6.14 (s, 3H), 6.22-6.31 (br q, 1H), 6.95 (s,1H), 7.14-7.24 (m, 6H), 7.31-7.39 (m, 9H), 7.45 (s, 1H).

(2-{2-[2-(11-Mercapto-undecanoylamino)-ethoxy]-ethoxy}-ethyl)-carbamicAcid 1-(4,5-Dimethoxy-2-nitro-phenyl)-ethyl Ester, HS(CH₂)₁₁(EG)₂NPOC(5). A solution of trifluoroacetic acid in dichloromethane (5% v/v), 4(1.2 g, 1.4 mmol), and triethylsilane (0.83 g, 7.1 mmol) was stirred for3 h at room temperature. The solution was washed with 0.2 M NaOH (2×100mL) and brine (2×100 mL), dried (MgSO₄), and evaporated to dryness. Thecrude compound was chromatographed (SiO₂/EtOAc→MeOH) to yield 0.46 g(0.77 mmol, 54%) of HS(CH₂)₁₁(EG)₂NPOC as a thick yellow oil.

HS(CH₂)₁₁(EG)₂NPOC, 5: ¹H NMR (CDCl₃, 500 MHz): ⊕1.24-1.42 (br s, 14H),1.57-1.68 (br t, 2H), 2.17-2.21 (br m, 2H), 2.51-2.57 (q, 2H), 3.32-3.41(m, 4H), 3.46-3.51 (m, 4H), 3.58-3.63 (m, 4H), 3.63-3.66 (s, 3H),3.66-3.69 (s, 3H), 6.14 (s, 3H), 6.22-6.31 (br q, 1H), 6.95 (s, 1H),7.45 (s, 1H). C₂₈H₄₇N₃O₉S (585.75): m/z 608.9 [M+Na⁺]+.

11-Tritylsulfanyl-undecanoic Acid[2-(2-{2-[2-(2,4-Dinitro-phenylamino)-acetylamino]-ethoxy}-ethoxy)-ethyl]-amide(6). To a stirred solution of 3 (0.25 g, 0.42 mmol) andN-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.1 g, 0.5mmol) in dichloromethane (50 mL) was added N-(2,4-dinitrophenyl)glycine(0.11 g, 0.51 mmol), and the solution was left to react at roomtemperature overnight. The solution was washed with 0.01 M HCl (1×100mL), 0.2 M NaOH (1×100 mL), and brine solution (1×100 mL). The solutionwas dried (MgSO₄) and evaporated to dryness. The crude compound waschromatographed (SiO₂/EtOAc→MeOH) to yield 0.26 g (0.33 mmol, 79%) of 6as a yellow oil. ¹H NMR (CDCl₃, 500 MHz): δ1.12-1.42 (br m, 14H),1.57-1.62 (br m, 2H), 1.63-1.72 (br t, 2H), 2.12-2.21 (br m, 2H),3.41-3.61 (br m, 12H), 4.17-4.21 (d, 2H), 5.87-5.92 (br s, 1H),6.89-6.94 (d, 1H), 7.14-7.24 (m, 6H),-7.31-7.39 (m, 9H), 8.26-8.32 (d,1H), 9.14-9.21 (br d, 1H). C₄₄H₅₅N₅O₈S (813.38): m/z 8.12.7 [M−H⁺]−.

11-Mercapto-undecanoic Acid[2-(2-{2-[2-(2,4-Dinitro-phenylamino)-acetylamino]-ethoxy}-ethoxy)-ethyl]-amide,HS(CH₂)₁₁(EG)₂DNP (7). A solution of trifluoroacetic acid indichloromethane (5% v/v), 6 (0.26 g, 0.33 mmol), and triethylsilane(0.19 g, 1.7 mmol) was stirred for 3 h at room temperature. The solutionwas washed with 0.2 M NaOH (2×100 mL) and brine (2×100 mL), dried(MgSO₄), and concentrated. The crude compound was chromatographed(SiO₂/EtOAc→MeOH) to yield 0.12 g (0.22 mmol, 67%) of HS(CH₂)₁₁(EG)₃DNPas an orange solid.

HS(CH₂)₁₁(EG)₂DNP, 7: ¹H NMR (CDCl₃, 500 MHz): δ1.22-11.39 (br s, 14H),1.58-1.65 (br t, 2H), 2.18-2.21 (br m, 2H), 2.52-2.56 (q, 2H), 3.41-3.49(m, 4H), 3.52-3.56 (m, 4H), 3.58-3.61 (m, 4H), 4.17-4.21 (d, 2H),6.89-6.94 (d, 1H), 8.26-8.32 (d, 1H), 9.14-9.21 (br d, 1H). C₂₅H₄₀N₄O₈S(571.69): m/z 594.8 [M+Na⁺]+.

Solid-Phase Synthesis of HS(CH₂)₁₁EG₆NPOP(GRGD) (8). The alkanethiolpeptide HS(CH₂)₁₁EG₆NPOP(GRGD), 8, was synthesized using Fmoc-tBuchemistry and stepwise solid-phase methodology (FIG. 2B). Synthesis ofprotected peptide chains was carried out on a 100-μmol scale startingfrom Fmoc-Asp(OtBu)-Wang resin. The Fmoc group was removed using 20%piperidine in dimethylformamide (DMF, 1×5 min, 1×15 min) under nitrogen.The resin was filtered and washed with DMF (6×3 min). For each couplingstep, a solution of the Fmoc-amino acid (5 equiv),(benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate(BOP, 5 equiv), and 1-hydroxybenzotriazole (HOBT, 5 equiv) in DMF andDIEA were added successively to the resin, and the suspension wasstirred for 10 min at room temperature. The coupling reaction wasmonitored using 2,4,6-trinitrobenzene sulfonic acid (TNBS). After theremoval of the last Fmoc protecting group, the resin was washed with DMFand TrS(CH₂)₁₁(EG)₆CH₂CO₂H (Prochimia, Poland; 2.5 equiv) was coupledusing BOP (2.5 equiv), HOBt (2.5 equiv), and DIEA (2.5 equiv) in DMF for5 h at room temperature. The resin was washed with dichloromethane anddiethyl ether and dried under nitrogen. Deprotection of the side chainand cleavage of the peptide from the resin were performed by treatmentwith TFA, dithiothreitol (DTT), water, and TIPS (triisopropyl-silane) inthe ratio 88:5:5:2 (TFA/DTT/H₂O/TIPS). After precipitation in cold etherand centrifugation, the deprotected peptide was solubilized andlyophilized. The crude peptide derivative was purified by HPLC (lineargradient, 0-80% B, 40 min) and lyophilized to yieldHS(CH₂)₁₁EG₆NPOP(GRGD) (8) as a white powder. HPLC t_(R) 18.84 min(linear gradient, 0-100% B, 20 min); MS (MALDI-TOF) m/z 1192.96 [M+1]+.

EXAMPLE2 Fabrication of the Photomask Used for Patterning Multiple,Aligned SAMs

This example describes the fabrication of a photomask that is selectiveto multiple wavelengths, having patterns of squares and triangles (seeFIG. 3). This photomask was used as both an area- andwavelength-selective filter. The squares (made in quartz) allowed allwavelengths of light to pass through; the triangles (made in indium tinoxide, ITO) allowed 365 nm light to pass through (but is essentiallyopaque to light at 220 nm), and the rest of the photomask was coveredwith chromium, which was opaque to all wavelengths of light used. Thephotomask, once fabricated, could be used repeatedly.

To demonstrate photopatterning of SAMs using two different wavelengthsof light from a Hg(Xe) arc lamp, a mask was fabricated with an array ofsquares in quartz and an array of triangles in ITO; the remainder of themask was rendered opaque using chromium (FIG. 3B). The photomask, oncefabricated, could be used repeatedly. The photomask was typically placed10-50 μm above the gold surface to avoid damaging SAMs on a surface,although only minimal damage (e.g., submicron scratches) was observed inexperiments where the mask was placed in contact with the SAM. Thephotomask was exposed to light at 220 nm (15 mW/cm², 15 min) and 365 nm(34 mW/cm², 3 min) in two separate steps because separate mirrors wereused to reflect these two wavelengths produced by the Hg(Xe). In otherembodiments, a single exposure could be used utilizing a mirror thatreflected light at 220 and 365 nm.

The example used a commercially available quartz substrate coated withITO (supplied by Delta Technologies, 1 mm thick substrate coated with˜200 nm of ITO, 15±5Ω) as the substrate for the photomask. A layer ofphotoresist (Shipley 1827, 2.7 μm thick) was spun on the substrate. Amask having patterns of squares and triangles was placed on top of thesubstrate, and this substrate was exposed, forming the pattern ofsquares and triangles (200 μm or 1 mm sides) in the photoresist. Usingelectron-beam metal evaporation, a film of chromium (100 nm thick) wasdeposited on top of the layer of photoresist. The photoresist wasdissolved using acetone (3 min) and the substrate was rinsed withisopropyl alcohol, leaving behind indium tin oxide in the square andtriangle regions, and chromium in regions that were not covered by thesquares and triangles. Using another layer of photoresist (Shipley 1827,2.7 μm thick) as an etch-mask, ITO was etched selectively in thesquares. The etchant solution for ITO consisted of deionized water, HCl,HNO₃ (15:4:1, v/v), and a few drops of Triton X-100 (55° C., 10 min).After etching, the substrate was rinsed with deionized water, and thephotoresist was removed using acetone (3 min). The substrate was thenrinsed with isopropyl alcohol.

A similar fabrication strategy was used for obtaining patterns ofmultiple, aligned SAMs that resist the adsorption of proteins. Thebackground region (that is not patterned with squares or triangles)comprised ITO, and the triangles comprised a 200 nm thick layer of goldon a 1 nm thick layer of titanium.

EXAMPLE 3 Patterning Multiple, Aligned SAMs Using Photolithography

This example describes the patterning of a gold substrate with threealigned regions of self-assembled monolayers (SAMs) using one photomaskand one set of exposures to light at different wavelengths, but withoutthe need for realignment of photomasks between exposures. This methoduses a polyfunctional alkanethiol that forms a SAM on a gold substrateand that presents two types of photocleavable bonds: a photocleavablegroup that cleaves on exposure to light at 365 nm and a thiolate bond(Au—S) that cleaves on exposure to light at 220 nm.

The multi-wavelength selective photomask was placed 10-50 μm above thegold surface containing the SAM, although the mask could also be placedin direct contact with the SAM. The photomask was exposed to light at220 nm (15 mW/cm², 15 min) and 365 nm (34 mW/cm², 3 min).

Two methods are described: the photopatterning method described by FIG.1A produced a SAM that terminates in amines after-exposure to light at365 nm, while the method described by FIG. 1B produced a SAM thatterminates in primary amides after exposure to light at 365 nm. Themethod described by FIG. 1B also permits the original SAM to presentarbitrary functionality beyond the photocleavable linker. A new SAM canbe formed in regions that are exposed to light at 220 nm in bothapproaches. R in the figure represents any group that can be coupled toa carboxylic acid, e.g., amine, alcohol, etc.; R′ in the figurerepresents any group that contains a carboxylic acid, aldehyde, etc.that can be coupled to an amine; R″ in the figure represents anarbitrary functionality that terminates with a thiol group. (Note:alkanethiol SAMs on gold substrates are tilted 30° to the normal and areshown here schematically without any tilt.)

The photopatterning method described by FIG. 1A produced a SAM thatterminates in amines after exposure to light at 365 nm. A photocleavableamine-protecting group, 1-(3,4-(methylenedioxy)-6-nitrophenyl)ethylchloroformate (MeNPOC, (CH₃O)₂C₆H₂NO₂CH(CH₃)OCOCl), which cleavesquantitatively on photolysis using near-UV light (365 nm) andregenerates the amines, was used (FIG. 1A). MeNPOC does not require theuse of solution-phase scavengers. In addition, it is possible to usethis surface for further modification: the amines generated bydeprotection can be modified using traditional solid-phase syntheticmethods.

A second method (FIG. 1B) used a photocleavable linker,3-[5-(1-amino-ethyl)-2-methoxy-4-nitro-phenoxy]-propionic acid (NPOP,H₂NCH(CH₃)C₆H₂(OCH₃)O(CH₂)₃CO₂H) and permited the alkanethiol to includefunctional groups beyond the photoclevable group. The o-nitrobenzylcomponent can be modified to present another chemical functionality,either before or after photopatterning. A SAM that contains NPOP andthat is exposed to light at 365 nm is converted to a SAM that terminatesin primary amides; these primary amides can, in certain embodiments, befunctionalized further (e.g., by reduction to amines with lithiumaluminum hydride), if desired.

EXAMPLE 4 Immunofluorescent Labeling of Photopatterned Mixed SAMs

This example describes the preparation and immunolabeling of a patternedsurface comprising multiple, aligned SAMs using mixed SAM-formingspecies of HS(CH₂)₁₁EG₂NPOC (5) and HS(CH₂)₁₁EG₆OH on a gold substrate(FIG. 4A).

To form a mixed SAM, gold was first evaporated on a glass slide (Ti, 1nm; Au, 30 nm). A mask (prepared by a procedure substantially similar tothat described in Example 2) was placed on top of a 50-μm Kapton spacerresting on the gold substrate and exposed to light at 365 nm (33.7mW/cm², 3 min) followed by an exposure to light at 220 nm (15 mW/cm², 15min). Upon exposure to light at both 220 and 365 nm through thephotomask (but without repositioning the mask or substrate between thetwo exposures), the mixed-SAM substrate was patterned into regionspresenting the original SAM, a SAM that terminated in primary amines,and bare gold.

The exposed gold surface was modified with a mixed SAM by incubationwith a solution containing HS(CH₂)₁₁EG₆OH (1.9 mM) and HS(CH₂)₁₁EG₂DNP(7) (0.1 mM; DNP, dinitrophenyl); the region that presented a SAM thatterminated in amines was modified by reaction with (+)-biotin (as the(+)-biotin N-hydroxysuccinimide ester, Biotin-NHS).

The gold substrate was incubated (60 s) in an ethanolic solution ofHS(CH₂)₁₁(EG)₃DNP (0.1 mM) and HS(CH₂)₁₁(EG)₆OH (1.9 mM), resulting inthe formation of a mixed SAM in the areas that had been exposed to 220nm light. The gold substrate was rinsed with ethanol.

Biotin-NHS was coupled to the amines in the region of the SAM that wasexposed to light at 365 nm only. To attach Biotin-NHS to the SAM,(+)-Biotin N-hydroxysuccinimide ester (5 mg, 15 μmol) was dissolved indimethyl sulfoxide (DMSO, 0.5 mL) and sonicated until a clear solutionwas obtained (60 s). The biotin-NHS solution was diluted immediatelybefore use with 50 mM sodium carbonate buffer (pH 9.55) to obtain a 1.5mM aqueous solution of biotin-NHS, and the gold substrate was incubated(300 s) in this aqueous solution. The substrate was rinsed with ethanoland dried with compressed nitrogen.

Surface blocking and antibody binding were carried out by successiveincubation steps (37° C., 1 h), each followed by rinsing with PBS, asfollows. Antibody solutions were diluted to their working concentrationusing blocking buffer. The substrate was incubated in blocking bufferand then incubated in a mixture of anti-DNP rabbit IgG (1:3.5) andanti-biotin mouse IgG (1:35).

A final incubation step was carried out in a mixture of fluorescentlylabeled anti-mouse IgG (AF488-anti-mouse IgG (1:10), green in FIG. 4B)and fluorescently labeled anti-rabbit IgG (TR-anti-rabbit IgG (1:10),blue in FIG. 4B). Using these antibodies, a fluorescence signal with anintensity that was indistinguishable from the background was recordedfrom the original SAM (black in FIG. 4B). (The gold substrate wasmounted on a coverslip using H-1000 mounting medium for fluorescence andimaged by fluorescence microscopy.) The resulting immunofluorescenceimage showed three aligned SAMs in the pattern of the photomask usedand, thus, demonstrated the ability to pattern multiple, aligned SAMsusing light and a photomask without alignment. A control experimentwhere anti-DNP rabbit IgG and anti-biotin mouse IgG were replaced byanti-BSA rabbit IgG (1:35) and anti-BSA mouse IgG (1:35) did not showany pattern. Thus, the image shown in FIG. 4B is a result of specificinteractions between antigens and antibodies.

EXAMPLE 5 Patterning and Characterization of Multiple Aligned SAMs ThatResist the Adsorption of Proteins

This example demonstrates the use of a SAM terminated in a peptidesequence, Gly-Arg-Gly-Asp (GRGD), which is linked to an alkanethiolcontaining a photocleavable moiety. The photocleavable moiety was usedto pattern two aligned SAMs that are resistant to the adsorption ofproteins, and a third region that does not resist the adsorption ofproteins. The RGD sequence is found within many extracellular matrix(ECM) proteins (fibronectin, laminin, vitronectin, collagens, andproteoglycans), and SAMs that incorporate this peptide sequence arerelevant for studies of adhesion of cells to surfaces.

A SAM was formed by incubating an electron-beam-deposited gold surfaceon a glass slide (Ti, 1 nm; Au, 30 nm) in an ethanolic solution ofHS(CH₂)₁₁EG₆NPOP(GRGD), 8 (0.05 mM) and HS(CH₂)₁₁EG₆OH (0.95 mM) over aperiod of 12 h (FIG. 5). Assuming that the concentration of alkanethiolsin solution approximates the concentration of alkanethiols in a SAM,this mixture of alkanethiols produced a SAM containing ˜5 mol %HS(CH₂)₁₁EG₆NPOP(GRGD) and 95 mol % HS(CH₂)₁₁EG₆OH (mol % refers to theratio of the number of moles of an individual alkanethiol relative tothe number of moles of both alkanethiols, expressed as a percentage). Infavorable cases, a mixed SAM that comprises at least 50 mol %HS(CH₂)₁₁EG₆OH resists the adsorption of proteins.

Using a procedure similar to that discussed above in Example 3 in thecontext of FIG. 1B, a mixed SAM of of HS(CH₂)₁₁EG₆NPOP(GRGD) andHS(CH₂)₁₁EG₆OH was illuminated through an area selective mask fabricatedin a manner similar to that described in Example 2. Upon exposure tolight at 365 nm (33.7 mW/cm², 3 min), the mixed SAM ofHS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH became HS(CH₂)₁₁EG₆CONH₂ andHS(CH₂)₁₁EG₆OH, respectively (FIG. 5A), and the surface remainedresistant to the adsorption of proteins. After exposure to light at 220nm (15 mW/cm², 15 min), the surface no longer resisted the adsorption ofproteins. The loss in ability to resist the adsorption of proteins afterexposure to-light at 220 nm was evidence that the SAM containingHS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH was photocleaved.

Using surface plasmon resonance (SPR) spectroscopy, the ability of SAMsexposed to different wavelengths of light to adsorb proteins wascharacterized. A SAM composed of hexadecanethiol on gold was used as aninternal standard; this SAM adsorbs a monolayer of protein, and thechange in reflectance due to this monolayer of protein is assigned avalue of 100% ML (ML, monolayer; i.e., one monolayer of adsorbedprotein). SPR established that a mixed SAM that was assumed to consistof 5 mol % HS(CH₂)₁₁EG₆NPOP(GRGD) and 95 mol % HS(CH₂)₁₁EG₆OH on a goldsubstrate was resistant to the adsorption of proteins prior toirradiation (FIG. 5B). Referring to FIG. 5B, an SPR sensorgram of themixed SAMs for substrates that have not been exposed to light, that havebeen exposed to light at 365 nm, and that have been exposed to light at220 nm is shown. The original SAM, protected from exposure to light bythe opaque, chromium area of the mask, remains resistant to theadsorption of fibrinogen (1 mg/mL, PBS buffer). After exposure to lightat 365 nm, the SAM region that terminates in primary amides resists theadsorption of proteins, and after exposure to light at 220 nm, the gold(or oxidized gold) surface (the monolayer is cleaved entirely) is unableto resist the adsorption of proteins.

It is noted that the amount of protein adsorbed on bare gold resulted inan increased % ML value compared with proteins adsorbed onhexadecanethiol SAMs. It is believed that proteins may become denaturedto a lesser extent on bare gold surfaces than on hexadecanethiol SAMs; adenatured protein probably presents a larger footprint on the surfaceand, in turn, limits the amount of protein adsorbed.

Surfaces were also characterized using MALDI-TOF MS (Su, J.; Mrksich, M.Angew. Chem., Int. Ed. 2002, 41, 4715-4718.; Su, J.; Mrksich, M.Langmuir 2003, 19, 4867-4870). FIG. 6 presents MALDI-TOF mass spectra ofsamples containing mixed SAMs that have not been exposed to light, thathave been exposed to light at 365 nm, and that have been exposed tolight at 220 nm. The peak at m/z 958 (a) corresponded to the symmetricdisulfide HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG6OH that is expected to be abundant inthe spectra of the mixed SAMs. The initial monolayer displayed a peak atm/z 1659 (II) corresponding to the asymmetric disulfideHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD) (expected m/z is 1659). Afterexposure to light at 365 nm, a peak at m/z 1015 (III) corresponding tothe asymmetric disulfide HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂ (expected m/z is992 plus Na⁺, m/z 23, gives m/z 1015) was observed. The presence of thepeak at m/z 1015 (III) and the absence of a peak at m/z 1659 (II)indicated the photocleavage of the peptide sequence and showed that theremaining SAM terminated in primary amides and hexaethylene glycolgroups. After exposure to light at 220 nm, no peaks were observed,indicating photocleavage of the mixed SAM. (No organic species with m/zgreater than 350, the lower limit of detection of the mass spectrometerused, was recorded from MS analysis of the SAM after exposure to lightat 220 nm.) No other molecular fragments are expected to be insignificant abundance in this region (800<m/z<2000) for all threespectra, in agreement with the observed data. The symmetric disulfides(GRGD)NPOPEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD) andH₂NOCEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂ are unlikely to appear in the massspectra because of the dilute concentration of the alkanethiolHS(CH₂)₁₁EG₆NPOP(GRGD) present in the original mixed SAM. Althoughindividual alkanethiols corresponding to HS(CH₂)₁₁EG₆NPOP(GRGD) andHS(CH₂)₁₁EG₆CONH₂ were observed occasionally, most molecular fragmentsappeared as disulfides.

Spatially resolved MALDI-TOF MS data were obtained by programming ascanner to obtain five mass spectra from 250 μm square regions acrossthe substrate. Each mass spectrum corresponded to either a regioncontaining the original SAM, the SAM after exposure to light at 365 nm,or the bare gold. For the purposes of presentation, an arbitrary colorwas assigned to each pixel: white for m/z signals representing theoriginal SAM (HOEG₆(CH₂)₁₁SS(CH₂)₁₁(EG₆NPOP(GRGD)), gray for m/z signalsrepresenting the SAM after exposure to light at 365 nm(HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂), and black for when no m/z signal wasdetected. A spatial representation of these data using the arbitraryvalues and their corresponding x-y coordinates was plotted.

A substrate was scanned that contained multiple, aligned SAMs (1 cm×1 cmsquare region) and the observed m/z peaks were plotted as a function ofposition on the substrate (FIG. 7). FIG. 7 illustrates that results forthe patterning of two regions of aligned SAMs that resist the adsorptionof proteins and a third region that does not resist the adsorption ofproteins. FIG. 7A illustrates a representation of the expected patternof multiple, aligned SAMs generated from a mixed SAM containingHS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH. FIG. 7B presents a spatiallyresolved image of multiple, aligned SAMs constructed from the locationof m/z peaks obtained using MALDI-TOF and corresponding toHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD) (white),HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂ (gray), or no alkanethiol (black). Thespatial resolution of the detector used was limited to 100 μm (seebelow).

The resolution of the resulting plot was limited to about 100 μm, sincethe spatial resolution of the detector used to acquire individual massspectra from the patterned substrate was limited to square pixels with adimension of 100 μm. The spatially resolved plot showed three distinctregions: the original SAM (m/z arising fromHOEG₆-(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD)), the SAM after exposure to light at365 nm (m/z arising from HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂), and the SAMafter exposure to light at 220 nm. The expected pattern of multiple,aligned SAMs generated using our photomask is shown in FIG. 7A, and theobserved plot of the multiple, aligned SAMs as generated from ananalysis of m/z peaks in MS data is shown in FIG. 7B. It may beconcluded from both the MS and SPR data that two regions of aligned SAMswere patterned that resist the adsorption of proteins and a third regionwas also patterned that does not resist the adsorption of proteins. Insummary, the patterning of multiple, aligned regions of alkanethiol SAMsthat resist the adsorption of proteins has been demonstrated.

Such multiple, aligned patterns of SAMs can be used, as but one of manyexamples, for patterning multiple cell types and for studying cell-cellsignaling (where one cell type is separated from the other on thesurface).

EXAMPLE 6

To demonstrate photopatterning of SAMs using two different wavelengthsof light from a lamp, such as an Hg(Xe) arc lamp, a mask was fabricatedcomprising an array of squares in quartz and an array of triangles inITO; the remainder of the mask was made opaque using chromium (FIG. 3B).The photomask, once fabricated, could be used repeatedly. In some cases,the photomask was placed 10-50 μm above the gold surface. In othercases, the photomask was placed in direct contact with the molecules onthe surface. In certain embodiments, generation of patterns comprisingmultiple, aligned molecules requires only a single exposure of light atmultiple wavelengths using a photomask having multiplewavelength-selective regions.

The ITO was etched for 10 min, which was found to be the optimal time toexpose a uniform quartz region; however, the etchant partially removedmetal near the quartz region, and a semitransparent region was producedaround metal regions that failed to absorb light at 220 and 365 nm asefficiently as metal that was not etched. These partially exposedregions of ITO are responsible for the blue border around the blackpattern in FIG. 4B.

A mixed SAM containing HS(CH₂)₁₁EG₂NPOC and HS(CH₂)₁₁EG₆OH on a goldsubstrate (FIG. 4A) was used to patterning multiple, aligned SAMs usingphotolithography. Upon exposure to light at both 220 and 365 nm throughthe photomask (but without repositioning the mask or substrate betweenthe two exposures), the substrate could be patterned into regionspresenting the original SAM, a SAM that terminated in primary amines,and bare gold. The region that presented a SAM that terminated in aminescould be modified, for example, by reaction with (+)-biotin (as the(+)-biotin N-hydroxysuccinimide ester), and the exposed gold surfacecould be modified, for example, with a mixed SAM by incubation with asolution containing HS(CH₂)₁₁EG₆OH (1.9 mM) and HS(CH₂)₁₁EG₂DNP (7) (0.1mM; DNP, dinitrophenyl). It should be understood that theamine-terminating region can be modified by any appropriate chemicalgroup, using any appropriate technique such as by chemical reaction,protein binding, van der Waals interaction, hydrogen bonding, orphysical adsorption. Similarly, the exposed gold surface can be modifiedby any SAM-forming species, or any technique such as the ones mentionedherein.

Surfaces containing the appropriate attached molecules could be used forspecific interactions, for example, for the binding interaction betweenantigens and antibodies. These surfaces could also be labeledimmunofluorescently. For example, the substrate mentioned above could beincubated with anti-biotin mouse IgG and anti-DNP rabbit IgG and thenwith a mixture of fluorescently labeled anti-mouse IgG (green in FIG.4B) and fluorescently labeled anti-rabbit IgG (blue in FIG. 4B). Usingthese antibodies, a fluorescence signal with an intensity that wasindistinguishable from the background was recorded from the original SAM(black in FIG. 4B). The resulting immunofluorescence image showed threealigned SAMs in the pattern of the photomask used and, thus,demonstrated the ability to pattern multiple, aligned SAMs using lightand a photomask without alignment. A control experiment where anti-DNPrabbit IgG and anti-biotin mouse IgG were replaced by anti-BSA rabbitIgG and anti-BSA mouse IgG did not show any pattern. Thus, it wasconcluded that the image shown in FIG. 4B is a result of specificinteractions between antigens and antibodies.

In certain cases, a photocleavable linker (FIG. 1B) that allowed thealkanethiol to include functional groups beyond the photocleavablelinker was used in the formation of mutliple, aligned molecules. Forexample, a peptide sequence, Gly-Arg-Gly-Asp (GRGD), was added to analkanethiol that comprised a photocleavable linker. The RGD sequence isfound within many extracellular matrix (ECM) proteins (fibronectin,laminin, vitronectin, collagens, and proteoglycans), and SAMs thatincorporate this peptide sequence are relevant for studies of adhesionof cells to surfaces. A SAM was formed from an ethanolic solution ofHS(CH₂)₁₁EG₆NPOP(GRGD), 8 (0.05 mM), and HS(CH₂)₁₁EG₆OH (0.95 mM) on agold substrate (FIG. 5). Assuming that the concentration of alkanethiolsin solution approximates the concentration of alkanethiols in a SAM,this mixture of alkanethiols produced a SAM containing ˜5 mol %HS(CH₂)₁₁EG₆NPOP(GRGD) and ˜95 mol % HS(CH₂)₁₁EG₆OH (mol % refers to theratio of the number of moles of an individual alkanethiol relative tothe number of moles of both alkanethiols, expressed as a percentage). Insome cases, a mixed SAM that comprises at least 50 mol % HS(CH₂)₁₁EG₆OHwas found to resist the adsorption of proteins.

In some cases, a photocleavable linker was used to pattern two alignedSAMs that are resistant to the adsorption of proteins and a third regionthat does not resist the adsorption of proteins. The two aligned SAMsthat were resistant to the adsorption of proteins contained, beforeexposure to light at 365 nm, HS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OHand, after exposure to light at 365 nm, HS(CH₂)₁₁EG₆CONH₂ andHS(CH₂)₁₁EG₆OH.

The ability of SAMs exposed to different wavelengths of light to adsorbproteins can be characterized using techniques such as surface plasmonresonance (SPR) spectroscopy. A SAM comprising hexadecanethiol on goldwas used as an internal standard; this SAM adsorbs a monolayer ofprotein, and the change in reflectance due to this monolayer of proteinis assigned a value of 100% ML (ML, monolayer; i.e., one monolayer ofadsorbed protein). SPR established that a mixed SAM we assumed tocomprise 5 mol % HS(CH₂)₁₁EG₆NPOP(GRGD) and 95 mol % HS(CH₂)₁₁EG₆OH on agold substrate was resistant to the adsorption of proteins prior toirradiation (FIG. 5). This mixed SAM was characterized after exposure tolight at 220 and 365 nm. After exposure to light at 365 nm, the surfaceremained resistant to the adsorption of proteins, and after exposure tolight at 220 nm, the surface no longer resisted the adsorption ofproteins. The loss in ability to resist the adsorption of proteins afterexposure to light at 220 nm was evidence that the SAM containingHS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH was photocleaved. It is notedthat the amount of protein adsorbed on bare gold results in an increased% ML value compared with proteins adsorbed on hexadecanethiol SAMs. Theproteins may be denatured to a lesser extent on bare gold surfaces thanon hexadecanethiol SAMs; a denatured protein may present a largerfootprint on the surface and, in turn, limits the amount of proteinadsorbed. From SPR, it was concluded that a mixed SAM comprisingHS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH (before exposure to light at365 nm) as well as a mixed SAM comprising HS(CH₂)₁₁EG₆CONH₂ andHS(CH₂)₁₁EG₆OH (after exposure to light at 365 nm) resisted theadsorption of proteins.

The surfaces described herein were also characterized using MALDI-TOFMS. MALDI-TOF MS provided the molecular weights of the components (asthe sodium adducts of disulfides, primarily) containing the original SAM(containing HS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH), the SAM afterexposure to light at 365 nm, and the SAM after exposure to light at 220nm (FIG. 6). In the case of the SAM before exposure to light at 365 and220 nm (containing HS(CH₂)₁₁EG₆NPOP(GRGD) and HS(CH₂)₁₁EG₆OH), a peak atm/z 1659 corresponded to the asymmetric disulfideHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD). After exposure to light at 365 nm, apeak appeared at m/z 1015, which corresponded to the asymmetricdisulfide HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂. The presence of this peak andthe absence of a peak at m/z 1659 indicated the photocleavage of thepeptide sequence and showed that the remaining SAM terminated in primaryamides and hexaethylene glycol groups. The peak at m/z 958, found ineach of the previous spectra, corresponded to the symmetric disulfideHOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆OH expected to be present in both samples. Sinceno organic species with m/z greater than 350 (lower limit of detectionof our mass spectrometer) was recorded from MS analysis of the SAM afterexposure to light at 220 nm, it was concluded that in regions exposed tolight at 220 nm, the entire SAM is photocleaved.

A substrate containing multiple, aligned SAMs (1 cm×1 cm square region)was scanned, and the observed m/z peaks as a function of position on thesubstrate was plotted (FIG. 7). The resolution of the resulting plot wasabout 100 μm in this example. The spatially resolved plot showed threedistinct regions: the original SAM (m/z arising fromHOEG₆-(CH₂)₁₁SS(CH₂)₁₁EG₆NPOP(GRGD)), the SAM after exposure to light at365 nm (m/z arising from HOEG₆(CH₂)₁₁SS(CH₂)₁₁EG₆CONH₂), and the SAMafter exposure to light at 220 nm. The expected pattern of multiple,aligned SAMs generated using the photomask is shown in FIG. 7A, and theobserved plot of the multiple, aligned SAMs as generated from ananalysis of m/z peaks in MS data is shown in FIG. 7B. From both the MSand SPR data, it can be concluded that two aligned SAMs that resist theadsorption of proteins and a third region that does not resist theadsorption of proteins was patterned. In summary, the patterning ofmultiple, aligned regions of alkanethiol SAMs that resist the adsorptionof proteins has been shown.

EXAMPLE 7 Multiple, Aligned SAMs Used as Etch Resists

This example illustrates that multiple, aligned molecules on surfacescan be used as etch resists. For example, SAMs formed from alkanethiolson gold can resist corrosion by solution-phase chemical etchants. Inthis example, a chrome adhesion layer was deposited on a siliconsubstrate, and a layer of gold was deposited on the adhesion layer. Thissubstrate was then incubated in an alkanethiol that included aphotocleavable group; exposure of this alkanethiol to 365 nm lightcleaved the right-hand portion of the molecule, leaving an amineend-group on the alkanethiol; exposure of the original alkanethiol to220 nm light cleaved the thiol-gold bond, leaving behind a bare goldregion on the substrate. The alkanethiol used in this example was:

and the cleaved portion had a structure:

After placing a photomask (that included regions that were transparentat both 220 nm and 365 nm light) on top of the substrate, the substratewas exposed to 220 nm and 365 nm light, and then exposed to an etchantsolution. FIG. 8 shows the result of the experiment. The continuous goldfilm represents a region protected from light at 220 nm and 365 nm. Thepartial gold film represents a region protected only from 220 nm light,and shows some degree of etching. The chrome/silicon region represents aregion exposed to light at 220 nm and 365 nm. Exposure times weresimilar to those in other experiments requiring exposure. Thus, thisexample shows that multiple, aligned molecules of discontinuous patternscan be made and used as etch resists on a surface.

While several embodiments of the present invention have been describedand illustrated herein, those of ordinary skill in the art will readilyenvision a variety of other means and/or structures for performing thefunctions and/or obtaining the results and/or one or more of theadvantages described herein, and each of such variations and/ormodifications is deemed to be within the scope of the present invention.More generally, those skilled in the art will readily appreciate thatall parameters, dimensions, materials, and configurations describedherein are meant to be exemplary and that the actual parameters,dimensions, materials, and/or configurations will depend upon thespecific application or applications for which the teachings of thepresent invention is/are used. Those skilled in the art will recognize,or be able to ascertain using no more than routine experimentation, manyequivalents to the specific embodiments of the invention describedherein. It is, therefore, to be understood that the foregoingembodiments are presented by way of example only and that, within thescope of the appended claims and equivalents thereto, the invention maybe practiced otherwise than as specifically described and claimed. Thepresent invention is directed to each individual feature, system,article, material, kit, and/or method described herein. In addition, anycombination of two or more such features, systems, articles, materials,kits, and/or methods, if such features, systems, articles, materials,kits, and/or methods are not mutually inconsistent, is included withinthe scope of the present invention.

All definitions, as defined and used herein, should be understood tocontrol over dictionary definitions, definitions in documentsincorporated by reference, and/or ordinary meanings of the definedterms.

The indefinite articles “a” and “an,” as used herein in thespecification and in the claims, unless clearly indicated to thecontrary, should be understood to mean “at least one.” The phrase“and/or,” as used herein in the specification and in the claims, shouldbe understood to mean “either or both” of the elements so conjoined,i.e., elements that are conjunctively present in some cases anddisjunctively present in other cases. Multiple elements listed with“and/or” should be construed in the same fashion, i.e., “one or more” ofthe elements so conjoined. Other elements may optionally be presentother than the elements specifically identified by the “and/or” clause,whether related or unrelated to those elements specifically identified.Thus, as a non-limiting example, a reference to “A and/or B”, when usedin conjunction with open-ended language such as “comprising” can refer,in one embodiment, to A only (optionally including elements other thanB); in another embodiment, to B only (optionally including elementsother than A); in yet another embodiment, to both A and B (optionallyincluding other elements); etc.

As used herein in the specification and in the claims, “or” should beunderstood to have the same meaning as “and/or” as defined above. Forexample, when separating items in a list, “or” or “and/or” shall beinterpreted as being inclusive, i.e., the inclusion of at least one, butalso including more than one, of a number or list of elements, and,optionally, additional unlisted items. Only terms clearly indicated tothe contrary, such as “only one of” or “exactly one of,” or, when usedin the claims, “consisting of,” will refer to the inclusion of exactlyone element of a number or list of elements. In general, the term “or”as used herein shall only be interpreted as indicating exclusivealternatives (i.e. “one or the other but not both”) when preceded byterms of exclusivity, such as “either,” “one of,” “only one of,” or“exactly one of.” “Consisting essentially of”, when used in the claims,shall have its ordinary meaning as used in the field of patent law.

As used herein in the specification and in the claims, the phrase “atleast one,” in reference to a list of one or more elements, should beunderstood to mean at least one element selected from any one or more ofthe elements in the list of elements, but not necessarily including atleast one of each and every element specifically listed within the listof elements and not excluding any combinations of elements in the listof elements. This definition also allows that elements may optionally bepresent other than the elements specifically identified within the listof elements to which the phrase “at least one” refers, whether relatedor unrelated to those elements specifically identified. Thus, as anon-limiting example, “at least one of A and B” (or, equivalently, “atleast one of A or B,” or, equivalently “at least one of A and/or B”) canrefer, in one embodiment, to at least one, optionally including morethan one, A, with no B present (and optionally including elements otherthan B); in another embodiment, to at least one, optionally includingmore than one, B, with no A present (and optionally including elementsother than A); in yet another embodiment, to at least one, optionallyincluding more than one, A, and at least one, optionally including morethan one, B (and optionally including other elements); etc.

It should also be understood that, unless clearly indicated to thecontrary, in any methods claimed herein that include more than one stepor act, the order of the steps or acts of the method is not necessarilylimited to the order in which the steps or acts of the method arerecited.

In the claims, as well as in the specification above, all transitionalphrases such as “comprising,” “including,” “carrying,” “having,”“containing,” “involving,” “holding,” “composed of,” and the like are tobe understood to be open-ended, i.e., to mean including but not limitedto. Only the transitional phrases “consisting of” and “consistingessentially of” shall be closed or semi-closed transitional phrases,respectively, as set forth in the United States Patent Office Manual ofPatent Examining Procedures, Section 2111.03.

1. A method comprising acts of: providing a surface, at least a portionof which comprises molecules attached thereon; exposing the surface toelectromagnetic radiation; and altering the layer of molecules with theelectromagnetic radiation to form a pattern comprising at least a first,second, and third region, wherein the first, second, and third regionsdiffer from each other in at least one chemical and/or physicalcharacteristic.
 2. A method as in claim 1, wherein the molecules arearranged on the surface in a layer.
 3. A method as in claim 2, whereinthe layer comprises a monolayer.
 4. A method as in claim 3, wherein themonolayer comprises a SAM.
 5. A method as in claim 1, wherein the first,second, and third regions differ from each other in theirhydrophobicity, ability to resist binding of proteins, ability to bindto cells, and/or ability to be etched by exposure to an etchingsolution.
 6. A method as in claim 1, wherein at least one of the first,second, and third regions of the pattern is non-continuous.
 7. A methodas in claim 1, wherein each of the first, second, and third regions ofthe pattern is non-continuous.
 8. A method as in claim 1, wherein the atleast a first, second, and third region of the pattern are formedsimultaneously.
 9. A method as in claim 8, wherein the pattern is formedupon exposing the surface to only a single exposure of theelectromagnetic radiation.
 10. A method as in claim 1, wherein theexposing act comprises exposing the surface to light of at least a firstwavelength and a second wavelength.
 11. A method as in claim 10, whereinthe exposing act comprises passing light through a photomask having afirst region that is substantially transparent to light at the firstwavelength but is not substantially transparent to light at the secondwavelength.
 12. A method as in claim 11, wherein the photomask comprisesa second region that is substantially transparent to light at the firstwavelength and to light at the second wavelength, and a third regionthat is not substantially transparent to light at the first or secondwavelengths.
 13. A method as in claim 1, wherein in the altering act,the pattern is formed by chemically and/or physically altering moleculesattached to the surface.
 14. A method as in claim 13, wherein at leastthe first region of the pattern is formed via cleavage of at least aportion a molecular species attached on the surface within the firstregion.
 15. A method as in claim 14, wherein at least the second regionof the pattern is formed via cleavage of at least a portion a molecularspecies attached on the surface within the second region.
 16. A methodas in claim 15, wherein a point of cleavage of the molecular speciesattached on the surface within the first region is different from apoint of cleavage of the molecular species attached on the surfacewithin the second region.
 17. A method as in claim 16, wherein the pointof cleavage of the molecular species attached on the surface within thesecond region comprises a bond formed between the surface and themolecular species.
 18. A method as in claim 13, further comprising afterthe altering act: exposing at least a portion of the surface withanother entity to form a new chemical species attached to the surface.19. A method as in claim 13, further comprising: exposing at least aportion of molecules that have been chemically and/or physically alteredin the altering step with another entity to form a new chemical speciesattached to the surface.
 20. A method as in claim 16, wherein themolecules attached to the surface comprise a SAM-forming species thathas been bound to the surface, so that the layer of molecules attachedto the surface comprises a SAM.
 21. A method as in claim 20, wherein thelayer of molecules comprises an alkane thiol that has been bound to thesurface.
 22. A method as in claim 21, wherein the surface comprises Au,Ag, Pt, Pd, and/or Cu.
 23. A method as in claim 20, wherein theSAM-forming species that has been bound to the surface comprises atleast a first photoclevable moiety that is able to be cleaved with lighthaving a first wavelength of at least 250 nm.
 24. A method as in claim23, wherein the SAM-forming species that has been bound to the surfacefurther comprises at least one bond connecting at least a portion of amolecule of the species to the surface that is able to be cleaved withlight having a wavelength of at least 200 nm but less than the firstwavelength.
 25. A method as in claim 23, wherein the SAM-forming speciesthat has been bound to the surface does not require presence ofscavenger molecules during photocleavage. 26-27. (canceled)
 28. A methodas recited in claim 16, wherein the molecules attached to the surfacecomprise a silane moiety containing species that has been bound to thesurface.
 29. A method as in claim 28, wherein the surface comprises Siatoms.
 30. A method as in claim 29, wherein the surface comprises glass.31. (canceled)
 32. A method as in claim 31, wherein at least one regionof the pattern is characterized by a smallest cross-sectional dimensionnot exceeding about 10 microns.
 33. A method as in claim 32, wherein atleast one region of the pattern is characterized by a smallestcross-sectional dimension not exceeding about 1 micron.
 34. (canceled)35. A composition, comprising: a compound having a structure:X—R-Q, wherein X is an attachment moiety able to chemically bind asurface, Q comprises a photocleavable moiety, and R is a moietyconnecting X and Q. 36-81. (canceled)
 82. An article, comprising:

wherein | comprises a surface, X is an attachment moiety able tochemically bind a surface, Q comprises a photocleavable moiety, and R isa moiety connecting X and Q, such that

is not:

83-96. (canceled)